Canonical Allele Identifier: CA1458739386

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727851G= , CM000666.2:g.54727851G=	GRCh38
NC_000004.11:g.55594017G= , CM000666.1:g.55594017G=	GRCh37
NC_000004.10:g.55288774G=	NCBI36
NG_007456.1:g.74857G= , LRG_307:g.74857G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1794G=	ENSP00000390987.3:p.Gly598=
ENST00000685269.1:n.1881G=
ENST00000686011.1:c.1791G=	ENSP00000509704.1:p.Gly597=
ENST00000687109.1:c.1806G=	ENSP00000509371.1:p.Gly602=
ENST00000687208.1:n.2218G=
ENST00000687246.1:c.1791G=	ENSP00000509114.1:p.Gly597=
ENST00000687265.1:n.1961G=
ENST00000687295.1:c.1791G=	ENSP00000509450.1:p.Gly597=
ENST00000689832.1:c.1806G=	ENSP00000509084.1:p.Gly602=
ENST00000689994.1:c.1293G=	ENSP00000509156.1:p.Gly431=
ENST00000690543.1:c.1794G=	ENSP00000508831.1:p.Gly598=
ENST00000690917.1:n.2021G=
ENST00000691361.1:n.713G=
ENST00000692783.1:c.1803G=	ENSP00000508733.1:p.Gly601=
ENST00000692991.1:n.1900G=
ENST00000288135.6:c.1803G= MANE Select	ENSP00000288135.6:p.Gly601=
ENST00000288135.5:c.1803G=	ENSP00000288135.5:p.Gly601=
ENST00000412167.6:c.1791G=	ENSP00000390987.2:p.Gly597=
NM_000222.2:c.1803G= , LRG_307t1:c.1803G=	NP_000213.1:p.Gly601=
NM_001093772.1:c.1791G=	NP_001087241.1:p.Gly597=
XM_005265740.1:c.1806G=	XP_005265797.1:p.Gly602=
XM_005265741.1:c.1806G=	XP_005265798.1:p.Gly602=
XM_005265742.1:c.1794G=	XP_005265799.1:p.Gly598=
XM_005265742.3:c.1794G=	XP_005265799.1:p.Gly598=
XM_017008178.1:c.1803G=	XP_016863667.1:p.Gly601=
XM_017008179.1:c.1794G=	XP_016863668.1:p.Gly598=
XM_017008180.1:c.1791G=	XP_016863669.1:p.Gly597=
NM_000222.3:c.1803G= MANE Select	NP_000213.1:p.Gly601=
NM_001093772.2:c.1791G=	NP_001087241.1:p.Gly597=
NM_001385284.1:c.1806G=	NP_001372213.1:p.Gly602=
NM_001385285.1:c.1803G=	NP_001372214.1:p.Gly601=
NM_001385286.1:c.1791G=	NP_001372215.1:p.Gly597=
NM_001385288.1:c.1794G=	NP_001372217.1:p.Gly598=
NM_001385290.1:c.1806G=	NP_001372219.1:p.Gly602=
NM_001385292.1:c.1794G=	NP_001372221.1:p.Gly598=