Canonical Allele Identifier: CA1458747259

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54736602_54736606delinsCTCTT , CM000666.2:g.54736602_54736606delinsCTCTT	GRCh38
NC_000004.11:g.55602768_55602772delinsCTCTT , CM000666.1:g.55602768_55602772delinsCTCTT	GRCh37
NC_000004.10:g.55297525_55297529delinsCTCTT	NCBI36
NG_007456.1:g.83608_83612delinsCTCTT , LRG_307:g.83608_83612delinsCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.2577_2581delinsCTCTT	ENSP00000390987.3:p.Phe859=
ENST00000684818.1:n.1281_1285delinsCTCTT
ENST00000685269.1:n.2667_2671delinsCTCTT
ENST00000686011.1:c.2574_2578delinsCTCTT	ENSP00000509704.1:p.Phe858=
ENST00000687109.1:c.2592_2596delinsCTCTT	ENSP00000509371.1:p.Phe864=
ENST00000687208.1:n.3001_3005delinsCTCTT
ENST00000687246.1:c.2454_2458delinsCTCTT	ENSP00000509114.1:p.Phe818=
ENST00000687265.1:n.2747_2751delinsCTCTT
ENST00000687295.1:c.2577_2581delinsCTCTT	ENSP00000509450.1:p.Phe859=
ENST00000688060.1:n.386_390delinsCTCTT
ENST00000689832.1:c.2589_2593delinsCTCTT	ENSP00000509084.1:p.Phe863=
ENST00000689994.1:c.2079_2083delinsCTCTT	ENSP00000509156.1:p.Phe693=
ENST00000690543.1:c.2580_2584delinsCTCTT	ENSP00000508831.1:p.Phe860=
ENST00000690917.1:n.2807_2811delinsCTCTT
ENST00000691361.1:n.1499_1503delinsCTCTT
ENST00000692301.1:n.1281_1285delinsCTCTT
ENST00000692783.1:c.2586_2590delinsCTCTT	ENSP00000508733.1:p.Phe862=
ENST00000692991.1:n.2686_2690delinsCTCTT
ENST00000288135.6:c.2589_2593delinsCTCTT MANE Select	ENSP00000288135.6:p.Phe863=
ENST00000288135.5:c.2589_2593delinsCTCTT	ENSP00000288135.5:p.Phe863=
ENST00000412167.6:c.2577_2581delinsCTCTT	ENSP00000390987.2:p.Phe859=
NM_000222.2:c.2589_2593delinsCTCTT , LRG_307t1:c.2589_2593delinsCTCTT	NP_000213.1:p.Phe863=
NM_001093772.1:c.2577_2581delinsCTCTT	NP_001087241.1:p.Phe859=
XM_005265740.1:c.2592_2596delinsCTCTT	XP_005265797.1:p.Phe864=
XM_005265741.1:c.2589_2593delinsCTCTT	XP_005265798.1:p.Phe863=
XM_005265742.1:c.2580_2584delinsCTCTT	XP_005265799.1:p.Phe860=
XM_005265742.3:c.2580_2584delinsCTCTT	XP_005265799.1:p.Phe860=
XM_017008178.1:c.2586_2590delinsCTCTT	XP_016863667.1:p.Phe862=
XM_017008179.1:c.2577_2581delinsCTCTT	XP_016863668.1:p.Phe859=
XM_017008180.1:c.2574_2578delinsCTCTT	XP_016863669.1:p.Phe858=
NM_000222.3:c.2589_2593delinsCTCTT MANE Select	NP_000213.1:p.Phe863=
NM_001093772.2:c.2577_2581delinsCTCTT	NP_001087241.1:p.Phe859=
NM_001385284.1:c.2592_2596delinsCTCTT	NP_001372213.1:p.Phe864=
NM_001385285.1:c.2586_2590delinsCTCTT	NP_001372214.1:p.Phe862=
NM_001385286.1:c.2574_2578delinsCTCTT	NP_001372215.1:p.Phe858=
NM_001385288.1:c.2580_2584delinsCTCTT	NP_001372217.1:p.Phe860=
NM_001385290.1:c.2589_2593delinsCTCTT	NP_001372219.1:p.Phe863=
NM_001385292.1:c.2577_2581delinsCTCTT	NP_001372221.1:p.Phe859=