Transcript #00026029 (NM_001379500.1, COL18A1 gene)

Transcript name transcript variant 4
Gene name COL18A1 (collagen, type XVIII, alpha 1)
Chromosome 21
Transcript - NCBI ID NM_001379500.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001366429.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks MANE select
Date created 2025-11-09 16:16:48 +01:00 (CET)
Date last edited N/A


Variants

69 entries on 1 page. Showing entries 1 - 69.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. 16i_25i c.(2436+1_2437-1)_(_?)del r.? p.?
-?/. - c.107-12647G>A r.(=) p.(=)
?/. - c.107-12533C>T r.(=) p.(=)
-?/. - c.107-12513del r.(=) p.(=)
-?/. - c.107-12354G>A r.(=) p.(=)
?/. - c.107-12353G>A r.(=) p.(=)
-?/. - c.107-11882C>A r.(=) p.(=)
-/. - c.107-11719C>T r.(=) p.(=)
?/. - c.107-11586del r.(=) p.(=)
-?/. - c.107-11576C>G r.(=) p.(=)
-?/. - c.107-11502G>A r.(=) p.(=)
?/. - c.198G>C r.(?) p.(Leu66=)
?/. - c.352A>G r.(?) p.(Met118Val)
-?/. - c.450C>T r.(?) p.(Ala150=)
?/. - c.530A>G r.(?) p.(Tyr177Cys)
-?/. - c.547T>C r.(?) p.(Phe183Leu)
?/. - c.577C>T r.(?) p.(Arg193Trp)
?/. - c.625G>A r.(?) p.(Gly209Arg)
-?/. - c.803C>A r.(?) p.(Ala268Glu)
-?/. - c.1098G>T r.(?) p.(Pro366=)
-?/. - c.1221G>A r.(?) p.(Pro407=)
-?/. - c.1249-3C>T r.spl? p.?
-?/. - c.1404C>T r.(?) p.(Phe468=)
-?/. - c.1453-3C>T r.spl? p.?
?/. - c.1454G>T r.(?) p.(Gly485Val)
?/. - c.1483C>T r.(?) p.(Pro495Ser)
?/. - c.1549G>A r.(?) p.(Gly517Arg)
?/. - c.1553C>A r.(?) p.(Pro518His)
-?/. - c.1611+10G>A r.(=) p.(=)
?/. - c.1628C>T r.(?) p.(Pro543Leu)
?/. - c.1852G>A r.(?) p.(Gly618Arg)
?/. - c.2113C>A r.(?) p.(Pro705Thr)
-?/. - c.2157+14G>A r.(=) p.(=)
+?/. - c.2378dup r.(?) p.(Pro795Serfs*69)
-?/. - c.2379G>A r.(?) p.(Pro793=)
-?/. - c.2464G>C r.(?) p.(Glu822Gln)
?/. - c.2510G>C r.(?) p.(Gly837Ala)
+/. - c.2558dup r.(?) p.(Pro854Serfs*10)
?/. - c.2569G>A r.(?) p.(Asp857Asn)
?/. - c.2666G>C r.(?) p.(Gly889Ala)
?/. - c.2674G>A r.(?) p.(Gly892Arg)
?/. - c.2743C>T r.(?) p.(Arg915*)
-?/. - c.2790C>T r.(?) p.(Gly930=)
-?/. - c.2821C>G r.(?) p.(Pro941Ala)
-/. - c.2823_2831del r.(?) p.(Pro947_Pro949del)
-?/. - c.2823_2832del r.(?) p.(Gly942Alafs*86)
+?/. - c.2823_2841del r.(?) p.(Gly942Alafs*83)
+?/. - c.2824_2825del r.(?) p.(Gly942Profs*144)
-?/. - c.2826_2842del r.(?) p.(Pro944Thrfs*137)
-?/. - c.2827_2841del r.(?) p.(Pro943_Pro947del)
-?/. - c.2827_2841del r.(?) p.(Pro943_Pro947del)
-/. - c.2832_2834del r.(?) p.(Gly945del)
-?/. - c.2869-9C>T r.(=) p.(=)
?/. - c.2878G>A r.(?) p.(Gly960Arg)
?/. - c.3053dup r.(?) p.(Gly1019Trpfs*68)
+?/. - c.3062dup r.(?) p.(Gly1022Trpfs*65)
+?/. - c.3087+1G>T r.spl? p.?
?/. - c.3166G>A r.(?) p.(Glu1056Lys)
-?/. - c.3187C>T r.(?) p.(Arg1063Cys)
?/. - c.3218T>C r.(?) p.(Leu1073Pro)
?/. - c.3313C>T r.(?) p.(Arg1105Trp)
?/. - c.3314G>A r.(?) p.(Arg1105Gln)
?/. - c.3349C>T r.(?) p.(Arg1117Trp)
?/. - c.3522_3524del r.(?) p.(Leu1175del)
?/. - c.3580C>T r.(?) p.(Arg1194Trp)
?/. - c.3608G>A r.(?) p.(Arg1203His)
?/. - c.3626G>A r.(?) p.(Arg1209His)
-?/. - c.3822C>T r.(?) p.(Ser1274=)
?/. - c.3920C>T r.(?) p.(Ser1307Leu)
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