Canonical Allele Identifier: CA356911461

Gene: KIT

Linked Data

• dbSNP Id: rs2109801114
• MyVariant Identifiers: chr4:g.55599254G>T (hg19) ; chr4:g.54733088G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54733088G>T , CM000666.2:g.54733088G>T	GRCh38
NC_000004.11:g.55599254G>T , CM000666.1:g.55599254G>T	GRCh37
NC_000004.10:g.55294011G>T	NCBI36
NG_007456.1:g.80094G>T , LRG_307:g.80094G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000412167.7:c.2368G>T	ENSP00000390987.3:p.Ala790Ser
ENST00000685269.1:n.2458G>T
ENST00000686011.1:c.2365G>T	ENSP00000509704.1:p.Ala789Ser
ENST00000687109.1:c.2383G>T	ENSP00000509371.1:p.Ala795Ser
ENST00000687208.1:n.2792G>T
ENST00000687246.1:c.2349+1090G>T	ENSP00000509114.1:n.2349+1090G>T
ENST00000687265.1:n.2538G>T
ENST00000687295.1:c.2368G>T	ENSP00000509450.1:p.Ala790Ser
ENST00000688060.1:n.177G>T
ENST00000688704.1:n.1392G>T
ENST00000689832.1:c.2380G>T	ENSP00000509084.1:p.Ala794Ser
ENST00000689994.1:c.1870G>T	ENSP00000509156.1:p.Ala624Ser
ENST00000690543.1:c.2371G>T	ENSP00000508831.1:p.Ala791Ser
ENST00000690917.1:n.2598G>T
ENST00000691361.1:n.1290G>T
ENST00000692783.1:c.2377G>T	ENSP00000508733.1:p.Ala793Ser
ENST00000692991.1:n.2477G>T
ENST00000288135.6:c.2380G>T MANE Select	ENSP00000288135.6:p.Ala794Ser
ENST00000288135.5:c.2380G>T	ENSP00000288135.5:p.Ala794Ser
ENST00000412167.6:c.2368G>T	ENSP00000390987.2:p.Ala790Ser
ENST00000512959.1:n.433G>T
NM_000222.2:c.2380G>T , LRG_307t1:c.2380G>T	NP_000213.1:p.Ala794Ser
NM_001093772.1:c.2368G>T	NP_001087241.1:p.Ala790Ser
XM_005265740.1:c.2383G>T	XP_005265797.1:p.Ala795Ser
XM_005265741.1:c.2380G>T	XP_005265798.1:p.Ala794Ser
XM_005265742.1:c.2371G>T	XP_005265799.1:p.Ala791Ser
XM_005265742.3:c.2371G>T	XP_005265799.1:p.Ala791Ser
XM_017008178.1:c.2377G>T	XP_016863667.1:p.Ala793Ser
XM_017008179.1:c.2368G>T	XP_016863668.1:p.Ala790Ser
XM_017008180.1:c.2365G>T	XP_016863669.1:p.Ala789Ser
NM_000222.3:c.2380G>T MANE Select	NP_000213.1:p.Ala794Ser
NM_001093772.2:c.2368G>T	NP_001087241.1:p.Ala790Ser
NM_001385284.1:c.2383G>T	NP_001372213.1:p.Ala795Ser
NM_001385285.1:c.2377G>T	NP_001372214.1:p.Ala793Ser
NM_001385286.1:c.2365G>T	NP_001372215.1:p.Ala789Ser
NM_001385288.1:c.2371G>T	NP_001372217.1:p.Ala791Ser
NM_001385290.1:c.2380G>T	NP_001372219.1:p.Ala794Ser
NM_001385292.1:c.2368G>T	NP_001372221.1:p.Ala790Ser