Canonical Allele Identifier: CA1458739501

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727924A= , CM000666.2:g.54727924A=	GRCh38
NC_000004.11:g.55594090A= , CM000666.1:g.55594090A=	GRCh37
NC_000004.10:g.55288847A=	NCBI36
NG_007456.1:g.74930A= , LRG_307:g.74930A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000412167.7:c.1867A=	ENSP00000390987.3:p.Lys623=
ENST00000685269.1:n.1954A=
ENST00000686011.1:c.1864A=	ENSP00000509704.1:p.Lys622=
ENST00000687109.1:c.1879A=	ENSP00000509371.1:p.Lys627=
ENST00000687208.1:n.2291A=
ENST00000687246.1:c.1864A=	ENSP00000509114.1:p.Lys622=
ENST00000687265.1:n.2034A=
ENST00000687295.1:c.1864A=	ENSP00000509450.1:p.Lys622=
ENST00000689832.1:c.1879A=	ENSP00000509084.1:p.Lys627=
ENST00000689994.1:c.1366A=	ENSP00000509156.1:p.Lys456=
ENST00000690543.1:c.1867A=	ENSP00000508831.1:p.Lys623=
ENST00000690917.1:n.2094A=
ENST00000691361.1:n.786A=
ENST00000692783.1:c.1876A=	ENSP00000508733.1:p.Lys626=
ENST00000692991.1:n.1973A=
ENST00000288135.6:c.1876A= MANE Select	ENSP00000288135.6:p.Lys626=
ENST00000288135.5:c.1876A=	ENSP00000288135.5:p.Lys626=
ENST00000412167.6:c.1864A=	ENSP00000390987.2:p.Lys622=
NM_000222.2:c.1876A= , LRG_307t1:c.1876A=	NP_000213.1:p.Lys626=
NM_001093772.1:c.1864A=	NP_001087241.1:p.Lys622=
XM_005265740.1:c.1879A=	XP_005265797.1:p.Lys627=
XM_005265741.1:c.1879A=	XP_005265798.1:p.Lys627=
XM_005265742.1:c.1867A=	XP_005265799.1:p.Lys623=
XM_005265742.3:c.1867A=	XP_005265799.1:p.Lys623=
XM_017008178.1:c.1876A=	XP_016863667.1:p.Lys626=
XM_017008179.1:c.1867A=	XP_016863668.1:p.Lys623=
XM_017008180.1:c.1864A=	XP_016863669.1:p.Lys622=
NM_000222.3:c.1876A= MANE Select	NP_000213.1:p.Lys626=
NM_001093772.2:c.1864A=	NP_001087241.1:p.Lys622=
NM_001385284.1:c.1879A=	NP_001372213.1:p.Lys627=
NM_001385285.1:c.1876A=	NP_001372214.1:p.Lys626=
NM_001385286.1:c.1864A=	NP_001372215.1:p.Lys622=
NM_001385288.1:c.1867A=	NP_001372217.1:p.Lys623=
NM_001385290.1:c.1879A=	NP_001372219.1:p.Lys627=
NM_001385292.1:c.1867A=	NP_001372221.1:p.Lys623=