Canonical Allele Identifier: CA1458739811

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54728099A= , CM000666.2:g.54728099A=	GRCh38
NC_000004.11:g.55594265A= , CM000666.1:g.55594265A=	GRCh37
NC_000004.10:g.55289022A=	NCBI36
NG_007456.1:g.75105A= , LRG_307:g.75105A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1959A=	ENSP00000390987.3:p.Leu653=
ENST00000685269.1:n.2046A=
ENST00000686011.1:c.1956A=	ENSP00000509704.1:p.Leu652=
ENST00000687109.1:c.1971A=	ENSP00000509371.1:p.Leu657=
ENST00000687208.1:n.2383A=
ENST00000687246.1:c.1956A=	ENSP00000509114.1:p.Leu652=
ENST00000687265.1:n.2126A=
ENST00000687295.1:c.1956A=	ENSP00000509450.1:p.Leu652=
ENST00000689832.1:c.1971A=	ENSP00000509084.1:p.Leu657=
ENST00000689994.1:c.1458A=	ENSP00000509156.1:p.Leu486=
ENST00000690543.1:c.1959A=	ENSP00000508831.1:p.Leu653=
ENST00000690917.1:n.2186A=
ENST00000691361.1:n.878A=
ENST00000692783.1:c.1968A=	ENSP00000508733.1:p.Leu656=
ENST00000692991.1:n.2065A=
ENST00000288135.6:c.1968A= MANE Select	ENSP00000288135.6:p.Leu656=
ENST00000288135.5:c.1968A=	ENSP00000288135.5:p.Leu656=
ENST00000412167.6:c.1956A=	ENSP00000390987.2:p.Leu652=
NM_000222.2:c.1968A= , LRG_307t1:c.1968A=	NP_000213.1:p.Leu656=
NM_001093772.1:c.1956A=	NP_001087241.1:p.Leu652=
XM_005265740.1:c.1971A=	XP_005265797.1:p.Leu657=
XM_005265741.1:c.1971A=	XP_005265798.1:p.Leu657=
XM_005265742.1:c.1959A=	XP_005265799.1:p.Leu653=
XM_005265742.3:c.1959A=	XP_005265799.1:p.Leu653=
XM_017008178.1:c.1968A=	XP_016863667.1:p.Leu656=
XM_017008179.1:c.1959A=	XP_016863668.1:p.Leu653=
XM_017008180.1:c.1956A=	XP_016863669.1:p.Leu652=
NM_000222.3:c.1968A= MANE Select	NP_000213.1:p.Leu656=
NM_001093772.2:c.1956A=	NP_001087241.1:p.Leu652=
NM_001385284.1:c.1971A=	NP_001372213.1:p.Leu657=
NM_001385285.1:c.1968A=	NP_001372214.1:p.Leu656=
NM_001385286.1:c.1956A=	NP_001372215.1:p.Leu652=
NM_001385288.1:c.1959A=	NP_001372217.1:p.Leu653=
NM_001385290.1:c.1971A=	NP_001372219.1:p.Leu657=
NM_001385292.1:c.1959A=	NP_001372221.1:p.Leu653=