Canonical Allele Identifier: CA1458738451

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727264C= , CM000666.2:g.54727264C=	GRCh38
NC_000004.11:g.55593430C= , CM000666.1:g.55593430C=	GRCh37
NC_000004.10:g.55288187C=	NCBI36
NG_007456.1:g.74270C= , LRG_307:g.74270C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1578C=	ENSP00000390987.3:p.Phe526=
ENST00000685269.1:n.1665C=
ENST00000686011.1:c.1575C=	ENSP00000509704.1:p.Phe525=
ENST00000687109.1:c.1590C=	ENSP00000509371.1:p.Phe530=
ENST00000687208.1:n.2002C=
ENST00000687246.1:c.1575C=	ENSP00000509114.1:p.Phe525=
ENST00000687265.1:n.1745C=
ENST00000687295.1:c.1575C=	ENSP00000509450.1:p.Phe525=
ENST00000689832.1:c.1590C=	ENSP00000509084.1:p.Phe530=
ENST00000689994.1:c.1077C=	ENSP00000509156.1:p.Phe359=
ENST00000690543.1:c.1578C=	ENSP00000508831.1:p.Phe526=
ENST00000690917.1:n.1805C=
ENST00000691361.1:n.497C=
ENST00000692783.1:c.1587C=	ENSP00000508733.1:p.Phe529=
ENST00000692991.1:n.1684C=
ENST00000288135.6:c.1587C= MANE Select	ENSP00000288135.6:p.Phe529=
ENST00000288135.5:c.1587C=	ENSP00000288135.5:p.Phe529=
ENST00000412167.6:c.1575C=	ENSP00000390987.2:p.Phe525=
NM_000222.2:c.1587C= , LRG_307t1:c.1587C=	NP_000213.1:p.Phe529=
NM_001093772.1:c.1575C=	NP_001087241.1:p.Phe525=
XM_005265740.1:c.1590C=	XP_005265797.1:p.Phe530=
XM_005265741.1:c.1590C=	XP_005265798.1:p.Phe530=
XM_005265742.1:c.1578C=	XP_005265799.1:p.Phe526=
XM_005265742.3:c.1578C=	XP_005265799.1:p.Phe526=
XM_017008178.1:c.1587C=	XP_016863667.1:p.Phe529=
XM_017008179.1:c.1578C=	XP_016863668.1:p.Phe526=
XM_017008180.1:c.1575C=	XP_016863669.1:p.Phe525=
NM_000222.3:c.1587C= MANE Select	NP_000213.1:p.Phe529=
NM_001093772.2:c.1575C=	NP_001087241.1:p.Phe525=
NM_001385284.1:c.1590C=	NP_001372213.1:p.Phe530=
NM_001385285.1:c.1587C=	NP_001372214.1:p.Phe529=
NM_001385286.1:c.1575C=	NP_001372215.1:p.Phe525=
NM_001385288.1:c.1578C=	NP_001372217.1:p.Phe526=
NM_001385290.1:c.1590C=	NP_001372219.1:p.Phe530=
NM_001385292.1:c.1578C=	NP_001372221.1:p.Phe526=