Canonical Allele Identifier: CA356911364

Gene: KIT

Linked Data

• MyVariant Identifiers: chr4:g.55599243A>C (hg19) ; chr4:g.54733077A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54733077A>C , CM000666.2:g.54733077A>C	GRCh38
NC_000004.11:g.55599243A>C , CM000666.1:g.55599243A>C	GRCh37
NC_000004.10:g.55294000A>C	NCBI36
NG_007456.1:g.80083A>C , LRG_307:g.80083A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000412167.7:c.2357A>C	ENSP00000390987.3:p.His786Pro
ENST00000685269.1:n.2447A>C
ENST00000686011.1:c.2354A>C	ENSP00000509704.1:p.His785Pro
ENST00000687109.1:c.2372A>C	ENSP00000509371.1:p.His791Pro
ENST00000687208.1:n.2781A>C
ENST00000687246.1:c.2349+1079A>C	ENSP00000509114.1:n.2349+1079A>C
ENST00000687265.1:n.2527A>C
ENST00000687295.1:c.2357A>C	ENSP00000509450.1:p.His786Pro
ENST00000688060.1:n.166A>C
ENST00000688704.1:n.1381A>C
ENST00000689832.1:c.2369A>C	ENSP00000509084.1:p.His790Pro
ENST00000689994.1:c.1859A>C	ENSP00000509156.1:p.His620Pro
ENST00000690543.1:c.2360A>C	ENSP00000508831.1:p.His787Pro
ENST00000690917.1:n.2587A>C
ENST00000691361.1:n.1279A>C
ENST00000692783.1:c.2366A>C	ENSP00000508733.1:p.His789Pro
ENST00000692991.1:n.2466A>C
ENST00000288135.6:c.2369A>C MANE Select	ENSP00000288135.6:p.His790Pro
ENST00000288135.5:c.2369A>C	ENSP00000288135.5:p.His790Pro
ENST00000412167.6:c.2357A>C	ENSP00000390987.2:p.His786Pro
ENST00000512959.1:n.422A>C
NM_000222.2:c.2369A>C , LRG_307t1:c.2369A>C	NP_000213.1:p.His790Pro
NM_001093772.1:c.2357A>C	NP_001087241.1:p.His786Pro
XM_005265740.1:c.2372A>C	XP_005265797.1:p.His791Pro
XM_005265741.1:c.2369A>C	XP_005265798.1:p.His790Pro
XM_005265742.1:c.2360A>C	XP_005265799.1:p.His787Pro
XM_005265742.3:c.2360A>C	XP_005265799.1:p.His787Pro
XM_017008178.1:c.2366A>C	XP_016863667.1:p.His789Pro
XM_017008179.1:c.2357A>C	XP_016863668.1:p.His786Pro
XM_017008180.1:c.2354A>C	XP_016863669.1:p.His785Pro
NM_000222.3:c.2369A>C MANE Select	NP_000213.1:p.His790Pro
NM_001093772.2:c.2357A>C	NP_001087241.1:p.His786Pro
NM_001385284.1:c.2372A>C	NP_001372213.1:p.His791Pro
NM_001385285.1:c.2366A>C	NP_001372214.1:p.His789Pro
NM_001385286.1:c.2354A>C	NP_001372215.1:p.His785Pro
NM_001385288.1:c.2360A>C	NP_001372217.1:p.His787Pro
NM_001385290.1:c.2369A>C	NP_001372219.1:p.His790Pro
NM_001385292.1:c.2357A>C	NP_001372221.1:p.His786Pro