Canonical Allele Identifier: CA123527

Gene: KIT

Linked Data

• ClinVar Variation Id: 13858
• ClinVar RCV Id: RCV000014872
• dbSNP Id: rs121913684
• COSMIC: COSM51381
• MyVariant Identifiers: chr4:g.55599260A>G (hg19) ; chr4:g.54733094A>G (hg38)
• PubMed: PMID:9450866

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54733094A>G , CM000666.2:g.54733094A>G	GRCh38
NC_000004.11:g.55599260A>G , CM000666.1:g.55599260A>G	GRCh37
NC_000004.10:g.55294017A>G	NCBI36
NG_007456.1:g.80100A>G , LRG_307:g.80100A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.2374A>G	ENSP00000390987.3:p.Arg792Gly
ENST00000685269.1:n.2464A>G
ENST00000686011.1:c.2371A>G	ENSP00000509704.1:p.Arg791Gly
ENST00000687109.1:c.2389A>G	ENSP00000509371.1:p.Arg797Gly
ENST00000687208.1:n.2798A>G
ENST00000687246.1:c.2349+1096A>G	ENSP00000509114.1:n.2349+1096A>G
ENST00000687265.1:n.2544A>G
ENST00000687295.1:c.2374A>G	ENSP00000509450.1:p.Arg792Gly
ENST00000688060.1:n.183A>G
ENST00000688704.1:n.1398A>G
ENST00000689832.1:c.2386A>G	ENSP00000509084.1:p.Arg796Gly
ENST00000689994.1:c.1876A>G	ENSP00000509156.1:p.Arg626Gly
ENST00000690543.1:c.2377A>G	ENSP00000508831.1:p.Arg793Gly
ENST00000690917.1:n.2604A>G
ENST00000691361.1:n.1296A>G
ENST00000692783.1:c.2383A>G	ENSP00000508733.1:p.Arg795Gly
ENST00000692991.1:n.2483A>G
ENST00000288135.6:c.2386A>G MANE Select	ENSP00000288135.6:p.Arg796Gly
ENST00000288135.5:c.2386A>G	ENSP00000288135.5:p.Arg796Gly
ENST00000412167.6:c.2374A>G	ENSP00000390987.2:p.Arg792Gly
ENST00000512959.1:n.439A>G
NM_000222.2:c.2386A>G , LRG_307t1:c.2386A>G	NP_000213.1:p.Arg796Gly
NM_001093772.1:c.2374A>G	NP_001087241.1:p.Arg792Gly
XM_005265740.1:c.2389A>G	XP_005265797.1:p.Arg797Gly
XM_005265741.1:c.2386A>G	XP_005265798.1:p.Arg796Gly
XM_005265742.1:c.2377A>G	XP_005265799.1:p.Arg793Gly
XM_005265742.3:c.2377A>G	XP_005265799.1:p.Arg793Gly
XM_017008178.1:c.2383A>G	XP_016863667.1:p.Arg795Gly
XM_017008179.1:c.2374A>G	XP_016863668.1:p.Arg792Gly
XM_017008180.1:c.2371A>G	XP_016863669.1:p.Arg791Gly
NM_000222.3:c.2386A>G MANE Select	NP_000213.1:p.Arg796Gly
NM_001093772.2:c.2374A>G	NP_001087241.1:p.Arg792Gly
NM_001385284.1:c.2389A>G	NP_001372213.1:p.Arg797Gly
NM_001385285.1:c.2383A>G	NP_001372214.1:p.Arg795Gly
NM_001385286.1:c.2371A>G	NP_001372215.1:p.Arg791Gly
NM_001385288.1:c.2377A>G	NP_001372217.1:p.Arg793Gly
NM_001385290.1:c.2386A>G	NP_001372219.1:p.Arg796Gly
NM_001385292.1:c.2374A>G	NP_001372221.1:p.Arg792Gly