Canonical Allele Identifier: CA1458759782

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54726114T= , CM000666.2:g.54726114T=	GRCh38
NC_000004.11:g.55592280T= , CM000666.1:g.55592280T=	GRCh37
NC_000004.10:g.55287037T=	NCBI36
NG_007456.1:g.73120T= , LRG_307:g.73120T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1531+76T=	ENSP00000390987.3:n.1531+76T=
ENST00000685269.1:n.1618+64T=
ENST00000686011.1:c.1528+76T=	ENSP00000509704.1:n.1528+76T=
ENST00000687109.1:c.1543+64T=	ENSP00000509371.1:n.1543+64T=
ENST00000687208.1:n.1955+64T=
ENST00000687246.1:c.1528+76T=	ENSP00000509114.1:n.1528+76T=
ENST00000687265.1:n.1698+76T=
ENST00000687295.1:c.1528+76T=	ENSP00000509450.1:n.1528+76T=
ENST00000689832.1:c.1543+64T=	ENSP00000509084.1:n.1543+64T=
ENST00000689994.1:c.1030+64T=	ENSP00000509156.1:n.1030+64T=
ENST00000690543.1:c.1531+76T=	ENSP00000508831.1:n.1531+76T=
ENST00000690917.1:n.1758+64T=
ENST00000691361.1:n.450+76T=
ENST00000692783.1:c.1540+64T=	ENSP00000508733.1:n.1540+64T=
ENST00000692991.1:n.1637+76T=
ENST00000288135.6:c.1540+64T= MANE Select	ENSP00000288135.6:n.1540+64T=
ENST00000288135.5:c.1540+64T=	ENSP00000288135.5:n.1540+64T=
ENST00000412167.6:c.1528+76T=	ENSP00000390987.2:n.1528+76T=
NM_000222.2:c.1540+64T= , LRG_307t1:c.1540+64T=	NP_000213.1:n.1540+64T=
NM_001093772.1:c.1528+76T=	NP_001087241.1:n.1528+76T=
XM_005265740.1:c.1543+64T=	XP_005265797.1:n.1543+64T=
XM_005265741.1:c.1543+64T=	XP_005265798.1:n.1543+64T=
XM_005265742.1:c.1531+76T=	XP_005265799.1:n.1531+76T=
XM_005265742.3:c.1531+76T=	XP_005265799.1:n.1531+76T=
XM_017008178.1:c.1540+64T=	XP_016863667.1:n.1540+64T=
XM_017008179.1:c.1531+76T=	XP_016863668.1:n.1531+76T=
XM_017008180.1:c.1528+76T=	XP_016863669.1:n.1528+76T=
NM_000222.3:c.1540+64T= MANE Select	NP_000213.1:n.1540+64T=
NM_001093772.2:c.1528+76T=	NP_001087241.1:n.1528+76T=
NM_001385284.1:c.1543+64T=	NP_001372213.1:n.1543+64T=
NM_001385285.1:c.1540+64T=	NP_001372214.1:n.1540+64T=
NM_001385286.1:c.1528+76T=	NP_001372215.1:n.1528+76T=
NM_001385288.1:c.1531+76T=	NP_001372217.1:n.1531+76T=
NM_001385290.1:c.1543+64T=	NP_001372219.1:n.1543+64T=
NM_001385292.1:c.1531+76T=	NP_001372221.1:n.1531+76T=