Canonical Allele Identifier: CA2586966013

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54728031_54728032insATGA , CM000666.2:g.54728031_54728032insATGA	GRCh38
NC_000004.11:g.55594197_55594198insATGA , CM000666.1:g.55594197_55594198insATGA	GRCh37
NC_000004.10:g.55288954_55288955insATGA	NCBI36
NG_007456.1:g.75037_75038insATGA , LRG_307:g.75037_75038insATGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000412167.7:c.1891_1892insATGA	ENSP00000390987.3:p.Arg631HisfsTer8
ENST00000685269.1:n.1978_1979insATGA
ENST00000686011.1:c.1888_1889insATGA	ENSP00000509704.1:p.Arg630HisfsTer8
ENST00000687109.1:c.1903_1904insATGA	ENSP00000509371.1:p.Arg635HisfsTer8
ENST00000687208.1:n.2315_2316insATGA
ENST00000687246.1:c.1888_1889insATGA	ENSP00000509114.1:p.Arg630HisfsTer8
ENST00000687265.1:n.2058_2059insATGA
ENST00000687295.1:c.1888_1889insATGA	ENSP00000509450.1:p.Arg630HisfsTer8
ENST00000689832.1:c.1903_1904insATGA	ENSP00000509084.1:p.Arg635HisfsTer8
ENST00000689994.1:c.1390_1391insATGA	ENSP00000509156.1:p.Arg464HisfsTer8
ENST00000690543.1:c.1891_1892insATGA	ENSP00000508831.1:p.Arg631HisfsTer8
ENST00000690917.1:n.2118_2119insATGA
ENST00000691361.1:n.810_811insATGA
ENST00000692783.1:c.1900_1901insATGA	ENSP00000508733.1:p.Arg634HisfsTer8
ENST00000692991.1:n.1997_1998insATGA
ENST00000288135.6:c.1900_1901insATGA MANE Select	ENSP00000288135.6:p.Arg634HisfsTer8
ENST00000288135.5:c.1900_1901insATGA	ENSP00000288135.5:p.Arg634HisfsTer8
ENST00000412167.6:c.1888_1889insATGA	ENSP00000390987.2:p.Arg630HisfsTer8
NM_000222.2:c.1900_1901insATGA , LRG_307t1:c.1900_1901insATGA	NP_000213.1:p.Arg634HisfsTer8
NM_001093772.1:c.1888_1889insATGA	NP_001087241.1:p.Arg630HisfsTer8
XM_005265740.1:c.1903_1904insATGA	XP_005265797.1:p.Arg635HisfsTer8
XM_005265741.1:c.1903_1904insATGA	XP_005265798.1:p.Arg635HisfsTer8
XM_005265742.1:c.1891_1892insATGA	XP_005265799.1:p.Arg631HisfsTer8
XM_005265742.3:c.1891_1892insATGA	XP_005265799.1:p.Arg631HisfsTer8
XM_017008178.1:c.1900_1901insATGA	XP_016863667.1:p.Arg634HisfsTer8
XM_017008179.1:c.1891_1892insATGA	XP_016863668.1:p.Arg631HisfsTer8
XM_017008180.1:c.1888_1889insATGA	XP_016863669.1:p.Arg630HisfsTer8
NM_000222.3:c.1900_1901insATGA MANE Select	NP_000213.1:p.Arg634HisfsTer8
NM_001093772.2:c.1888_1889insATGA	NP_001087241.1:p.Arg630HisfsTer8
NM_001385284.1:c.1903_1904insATGA	NP_001372213.1:p.Arg635HisfsTer8
NM_001385285.1:c.1900_1901insATGA	NP_001372214.1:p.Arg634HisfsTer8
NM_001385286.1:c.1888_1889insATGA	NP_001372215.1:p.Arg630HisfsTer8
NM_001385288.1:c.1891_1892insATGA	NP_001372217.1:p.Arg631HisfsTer8
NM_001385290.1:c.1903_1904insATGA	NP_001372219.1:p.Arg635HisfsTer8
NM_001385292.1:c.1891_1892insATGA	NP_001372221.1:p.Arg631HisfsTer8