Canonical Allele Identifier: CA891841856

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727495_54727497delinsCTT , CM000666.2:g.54727495_54727497delinsCTT	GRCh38
NC_000004.11:g.55593661_55593663delinsCTT , CM000666.1:g.55593661_55593663delinsCTT	GRCh37
NC_000004.10:g.55288418_55288420delinsCTT	NCBI36
NG_007456.1:g.74501_74503delinsCTT , LRG_307:g.74501_74503delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1718_1720delinsCTT	ENSP00000390987.3:p.Leu573_Pro574delinsProSer
ENST00000685269.1:n.1805_1807delinsCTT
ENST00000686011.1:c.1715_1717delinsCTT	ENSP00000509704.1:p.Leu572_Pro573delinsProSer
ENST00000687109.1:c.1730_1732delinsCTT	ENSP00000509371.1:p.Leu577_Pro578delinsProSer
ENST00000687208.1:n.2142_2144delinsCTT
ENST00000687246.1:c.1715_1717delinsCTT	ENSP00000509114.1:p.Leu572_Pro573delinsProSer
ENST00000687265.1:n.1885_1887delinsCTT
ENST00000687295.1:c.1715_1717delinsCTT	ENSP00000509450.1:p.Leu572_Pro573delinsProSer
ENST00000689832.1:c.1730_1732delinsCTT	ENSP00000509084.1:p.Leu577_Pro578delinsProSer
ENST00000689994.1:c.1217_1219delinsCTT	ENSP00000509156.1:p.Leu406_Pro407delinsProSer
ENST00000690543.1:c.1718_1720delinsCTT	ENSP00000508831.1:p.Leu573_Pro574delinsProSer
ENST00000690917.1:n.1945_1947delinsCTT
ENST00000691361.1:n.637_639delinsCTT
ENST00000692783.1:c.1727_1729delinsCTT	ENSP00000508733.1:p.Leu576_Pro577delinsProSer
ENST00000692991.1:n.1824_1826delinsCTT
ENST00000288135.6:c.1727_1729delinsCTT MANE Select	ENSP00000288135.6:p.Leu576_Pro577delinsProSer
ENST00000288135.5:c.1727_1729delinsCTT	ENSP00000288135.5:p.Leu576_Pro577delinsProSer
ENST00000412167.6:c.1715_1717delinsCTT	ENSP00000390987.2:p.Leu572_Pro573delinsProSer
NM_000222.2:c.1727_1729delinsCTT , LRG_307t1:c.1727_1729delinsCTT	NP_000213.1:p.Leu576_Pro577delinsProSer
NM_001093772.1:c.1715_1717delinsCTT	NP_001087241.1:p.Leu572_Pro573delinsProSer
XM_005265740.1:c.1730_1732delinsCTT	XP_005265797.1:p.Leu577_Pro578delinsProSer
XM_005265741.1:c.1730_1732delinsCTT	XP_005265798.1:p.Leu577_Pro578delinsProSer
XM_005265742.1:c.1718_1720delinsCTT	XP_005265799.1:p.Leu573_Pro574delinsProSer
XM_005265742.3:c.1718_1720delinsCTT	XP_005265799.1:p.Leu573_Pro574delinsProSer
XM_017008178.1:c.1727_1729delinsCTT	XP_016863667.1:p.Leu576_Pro577delinsProSer
XM_017008179.1:c.1718_1720delinsCTT	XP_016863668.1:p.Leu573_Pro574delinsProSer
XM_017008180.1:c.1715_1717delinsCTT	XP_016863669.1:p.Leu572_Pro573delinsProSer
NM_000222.3:c.1727_1729delinsCTT MANE Select	NP_000213.1:p.Leu576_Pro577delinsProSer
NM_001093772.2:c.1715_1717delinsCTT	NP_001087241.1:p.Leu572_Pro573delinsProSer
NM_001385284.1:c.1730_1732delinsCTT	NP_001372213.1:p.Leu577_Pro578delinsProSer
NM_001385285.1:c.1727_1729delinsCTT	NP_001372214.1:p.Leu576_Pro577delinsProSer
NM_001385286.1:c.1715_1717delinsCTT	NP_001372215.1:p.Leu572_Pro573delinsProSer
NM_001385288.1:c.1718_1720delinsCTT	NP_001372217.1:p.Leu573_Pro574delinsProSer
NM_001385290.1:c.1730_1732delinsCTT	NP_001372219.1:p.Leu577_Pro578delinsProSer
NM_001385292.1:c.1718_1720delinsCTT	NP_001372221.1:p.Leu573_Pro574delinsProSer