Transcript #00005190 (NM_000246.3, CIITA gene)

Transcript name class II, major histocompatibility complex, transactivator
Gene name CIITA (class II, major histocompatibility complex, transactivator)
Chromosome 16
Transcript - NCBI ID NM_000246.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000237.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

72 entries on 1 page. Showing entries 1 - 72.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.52+12G>A r.(=) p.(=)
./. - c.52+641C>G r.(=) p.(=)
./. - c.52+641C>G r.(=) p.(=)
-?/. - c.129C>T r.(?) p.(Asp43=)
-/. - c.200-10T>C r.(=) p.(=)
?/. - c.268G>C r.(?) p.(Glu90Gln)
-?/. - c.286G>A r.(?) p.(Ala96Thr)
?/. - c.286G>A r.(?) p.(Ala96Thr)
-?/. - c.354T>C r.(?) p.(Ile118=)
-?/. - c.358+11G>A r.(=) p.(=)
-/. - c.370C>A r.(?) p.(Pro124Thr)
?/. - c.455C>T r.(?) p.(Pro152Leu)
-?/. - c.479C>T r.(?) p.(Pro160Leu)
-/. - c.520= r.(=) p.(Gly174=)
-?/. - c.532G>A r.(?) p.(Asp178Asn)
-?/. - c.541A>G r.(?) p.(Thr181Ala)
-?/. - c.592G>A r.(?) p.(Gly198Ser)
-?/. - c.629-3C>T r.spl? p.?
?/. - c.647C>G r.(?) p.(Ser216Trp)
-/. - c.691C>T r.(?) p.(Pro231Ser)
-?/. - c.691C>T r.(?) p.(Pro231Ser)
-?/. - c.772+8C>T r.(=) p.(=)
-?/. - c.773-18T>G r.(=) p.(=)
+?/. - c.773-2A>G r.spl? p.?
-?/. - c.1054G>A r.(?) p.(Glu352Lys)
-?/. - c.1068G>A r.(?) p.(Pro356=)
-?/. - c.1068G>A r.(?) p.(Pro356=)
?/. - c.1169G>A r.(?) p.(Arg390Gln)
-?/. - c.1556C>T r.(?) p.(Pro519Leu)
-?/. - c.1572C>T r.(?) p.(Ser524=)
?/. - c.1588G>A r.(?) p.(Ala530Thr)
?/. - c.1591G>A r.(?) p.(Gly531Ser)
?/. - c.1591G>A r.(?) p.(Gly531Ser)
-?/. - c.1591G>A r.(?) p.(Gly531Ser)
-?/. - c.1683C>T r.(?) p.(Asp561=)
?/. - c.1907C>T r.(?) p.(Thr636Met)
?/. - c.1907C>T r.(?) p.(Thr636Met)
-?/. - c.1926C>T r.(?) p.(Val642=)
-?/. - c.1926C>T r.(?) p.(Val642=)
?/. - c.2028G>C r.(?) p.(Gln676His)
-?/. - c.2072C>A r.(?) p.(Ala691Asp)
-/. - c.2072C>A r.(?) p.(Ala691Asp)
-?/. - c.2072C>A r.(?) p.(Ala691Asp)
-?/. - c.2096C>T r.(?) p.(Pro699Leu)
-?/. - c.2113G>A r.(?) p.(Glu705Lys)
?/. - c.2113G>A r.(?) p.(Glu705Lys)
+?/. - c.2215_2233del r.(?) p.(Leu739Glyfs*17)
+?/. - c.2250G>A r.(?) p.(Trp750Ter)
-?/. - c.2436C>T r.(?) p.(Cys812=)
-?/. - c.2448C>T r.(?) p.(Ala816=)
-?/. - c.2448C>T r.(?) p.(Ala816=)
-?/. - c.2538T>C r.(?) p.(His846=)
-?/. - c.2606G>A r.(?) p.(Cys869Tyr)
-?/. - c.2617T>C r.(?) p.(Leu873=)
?/. - c.2620G>T r.(?) p.(Gly874Trp)
-?/. - c.2651G>A r.(?) p.(Arg884His)
-/. - c.2657+127C>G r.(=) p.(=)
-/. - c.2676G>A r.(?) p.(Thr892=)
-?/. - c.2682G>A r.(?) p.(Ala894=)
-/. - c.2699A>G r.(?) p.(Gln900Arg)
-?/. - c.2778G>A r.(?) p.(Lys926=)
-?/. - c.2884T>C r.(?) p.(Phe962Leu)
-?/. - c.2892G>A r.(?) p.(Leu964=)
?/. - c.3014C>G r.(?) p.(Ser1005Trp)
?/. - c.3052G>A r.(?) p.(Glu1018Lys)
-?/. - c.3062+14G>A r.(=) p.(=)
-?/. - c.3066G>A r.(?) p.(Leu1022=)
?/. - c.3174C>T r.(?) p.(Asp1058=)
?/. - c.3196C>T r.(?) p.(Arg1066Cys)
?/. - c.3207G>A r.(?) p.(Pro1069=)
-?/. - c.3344G>A r.(?) p.(Ser1115Asn)
-?/. - c.*735G>A r.(=) p.(=)
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