Transcript #00002053 (NM_000020.2, ACVRL1 gene)

Transcript name transcript variant 1
Gene name ACVRL1 (activin A receptor type II-like 1)
Chromosome 12
Transcript - NCBI ID NM_000020.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000011.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

133 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-129G>A r.(=) p.(=)
-/. - c.-5-33C>T r.(=) p.(=)
+/. 9i c.1348-769::? r.? p.?
-?/. - c.62-15C>T r.(=) p.(=)
-?/. - c.87C>T r.(?) p.(Gly29=)
-?/. - c.87C>T r.(?) p.(Gly29=)
-?/. - c.88C>T r.(?) p.(Pro30Ser)
+/. - c.106T>C r.(?) p.(Cys36Arg)
?/. - c.136T>G r.(?) p.(Cys46Gly)
+?/. 3 c.137G>T r.(?) p.(Cys46Phe)
?/. - c.142G>A r.(?) p.(Gly48Arg)
?/. - c.170G>A r.(?) p.(Arg57Gln)
?/. - c.170G>A r.(?) p.(Arg57Gln)
-?/. - c.170G>A r.(?) p.(Arg57Gln)
+/. - c.199C>T r.(?) p.(Arg67Trp)
-/. - c.207C>T r.(?) p.(Cys69=)
-?/. - c.207C>T r.(?) p.(Cys69=)
-/. - c.207C>T r.(?) p.(Cys69=)
-/. - c.207C>T r.(?) p.(Cys69=)
-?/. - c.207C>T r.(?) p.(Cys69=)
+/. - c.286A>G r.(?) p.(Asn96Asp)
+/. - c.313+1G>A r.spl? p.?
-/. - c.313+11C>T r.(=) p.(=)
-/. - c.313+11C>T r.(=) p.(=)
-/. - c.313+11C>T r.(=) p.(=)
-/. - c.313+11C>T r.(=) p.(=)
-/. - c.314-35A>G r.(=) p.(=)
?/. - c.321A>C r.(?) p.(Gln107His)
-/. - c.330G>A r.(?) p.(Ser110=)
-/. - c.330G>A r.(?) p.(Ser110=)
+/. - c.340G>T r.(?) p.(Gly114Ter)
+/. - c.352C>T r.(?) p.(Gln118Ter)
-?/. - c.376G>A r.(?) p.(Val126Met)
+/. - c.430C>T r.(?) p.(Arg144Ter)
+/. - c.439C>T r.(?) p.(Gln147Ter)
+/. - c.439C>T r.(?) p.(Gln147Ter)
+/. - c.474A>T r.spl p.(Gly158=)
?/. - c.511G>A r.(?) p.(Asp171Asn)
?/. - c.526-13T>A r.(=) p.(=)
?/. - c.599G>A r.(?) p.(Arg200Gln)
+?/. - c.625G>C r.(?) p.(Gly209Arg)
+/. 5i c.625+5G>C r.spl? p.?
-/. - c.626-59del r.(=) p.(=)
-/. - c.626-59G>T r.(=) p.(=)
-?/. - c.626-19C>T r.(=) p.(=)
+/. - c.626-3C>G r.spl? p.?
?/. - c.643G>A r.(?) p.(Glu215Lys)
?/. - c.647T>C r.(?) p.(Val216Ala)
?/. - c.652C>T r.(?) p.(Arg218Trp)
?/. - c.655G>C r.(?) p.(Gly219Arg)
-/. - c.664C>T r.(?) p.(His222Tyr)
-?/. - c.666C>T r.(?) p.(His222=)
?/. - c.666C>T r.(?) p.(His222=)
-?/. - c.669T>G r.(?) p.(Gly223=)
?/. - c.682G>A r.(?) p.(Val228Ile)
+?/. 6 c.692_694del r.(?) p.(Phe231del)
-/. - c.747G>A r.(?) p.(Val249=)
-/. - c.747G>A r.(?) p.(Val249=)
-/. - c.747G>A r.(?) p.(Val249=)
+?/. - c.773G>A r.(?) p.(Gly258Asp)
+/. - c.818T>C r.(?) p.(Leu273Pro)
?/. - c.841G>C r.(?) p.(Glu281Gln)
+/. - c.858C>A r.(?) p.(Tyr286Ter)
+/. - c.926del r.(?) p.(Gly309Alafs*45)
?/. - c.926G>T r.(?) p.(Gly309Val)
+?/. - c.938T>A r.(?) p.(Leu313Gln)
+?/. - c.950T>G r.(?) p.(Ile317Ser)
+?/. - c.986G>A r.(?) p.(Arg329His)
+/. - c.988G>A r.(?) p.(Asp330Asn)
+?/. - c.988G>T r.(?) p.(Asp330Tyr)
-/. - c.993C>T r.(?) p.(Phe331=)
+?/. - c.1003A>G r.(?) p.(Asn335Asp)
?/. - c.1022A>G r.(?) p.(Asn341Ser)
+/. - c.1042del r.(?) p.(Asp348Thrfs*6)
+/. - c.1048+42G>A r.(=) p.(=)
?/. - c.1103C>T r.(?) p.(Pro368Leu)
?/. - c.1112G>A r.(?) p.(Gly371Asp)
?/. - c.1120C>T r.(?) p.(Arg374Trp)
+/. - c.1121G>A r.(?) p.(Arg374Gln)
+/. - c.1126A>G r.(?) p.(Met376Val)
?/. - c.1127T>C r.(?) p.(Met376Thr)
-?/. - c.1131A>G r.(?) p.(Ala377=)
-?/. - c.1131A>G r.(?) p.(Ala377=)
+/. - c.1135G>A r.(?) p.(Glu379Lys)
?/. - c.1147G>T r.(?) p.(Glu383Ter)
?/. - c.1182G>C r.(?) p.(Lys394Asn)
?/. - c.1188T>A r.(?) p.(Thr396=)
+/. - c.1189G>A r.(?) p.(Asp397Asn)
+?/. - c.1198G>C r.(?) p.(Ala400Pro)
+/. - c.1231C>T r.(?) p.(Arg411Trp)
+/. - c.1231C>T r.(?) p.(Arg411Trp)
+/. - c.1232G>A r.(?) p.(Arg411Gln)
+/. - c.1232G>A r.(?) p.(Arg411Gln)
+/. - c.1232G>A r.(?) p.(Arg411Gln)
+/. - c.1232G>A r.(?) p.(Arg411Gln)
-?/. - c.1239C>T r.(?) p.(=)
+/. - c.1246G>A r.(?) p.(Gly416Ser)
-/. - c.1246+9C>T r.(=) p.(=)
-/. - c.1246+9C>T r.(=) p.(=)
-/. - c.1246+18A>C r.(=) p.(=)
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