Canonical Allele Identifier: CA645516947

Gene: KIT

Linked Data

• COSMIC: COSM24691

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54733154_54733155insTCATAG , CM000666.2:g.54733154_54733155insTCATAG	GRCh38
NC_000004.11:g.55599320_55599321insTCATAG , CM000666.1:g.55599320_55599321insTCATAG	GRCh37
NC_000004.10:g.55294077_55294078insTCATAG	NCBI36
NG_007456.1:g.80160_80161insTCATAG , LRG_307:g.80160_80161insTCATAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.2434_2435insTCATAG	ENSP00000390987.3:p.Arg811_Asp812insValIle
ENST00000685269.1:n.2524_2525insTCATAG
ENST00000686011.1:c.2431_2432insTCATAG	ENSP00000509704.1:p.Arg810_Asp811insValIle
ENST00000687109.1:c.2449_2450insTCATAG	ENSP00000509371.1:p.Arg816_Asp817insValIle
ENST00000687208.1:n.2858_2859insTCATAG
ENST00000687246.1:c.2349+1156_2349+1157insTCATAG	ENSP00000509114.1:n.2349+1156_2349+1157insTCATAG
ENST00000687265.1:n.2604_2605insTCATAG
ENST00000687295.1:c.2434_2435insTCATAG	ENSP00000509450.1:p.Arg811_Asp812insValIle
ENST00000688060.1:n.243_244insTCATAG
ENST00000688704.1:n.1458_1459insTCATAG
ENST00000689832.1:c.2446_2447insTCATAG	ENSP00000509084.1:p.Arg815_Asp816insValIle
ENST00000689994.1:c.1936_1937insTCATAG	ENSP00000509156.1:p.Arg645_Asp646insValIle
ENST00000690543.1:c.2437_2438insTCATAG	ENSP00000508831.1:p.Arg812_Asp813insValIle
ENST00000690917.1:n.2664_2665insTCATAG
ENST00000691361.1:n.1356_1357insTCATAG
ENST00000692783.1:c.2443_2444insTCATAG	ENSP00000508733.1:p.Arg814_Asp815insValIle
ENST00000692991.1:n.2543_2544insTCATAG
ENST00000288135.6:c.2446_2447insTCATAG MANE Select	ENSP00000288135.6:p.Arg815_Asp816insValIle
ENST00000288135.5:c.2446_2447insTCATAG	ENSP00000288135.5:p.Arg815_Asp816insValIle
ENST00000412167.6:c.2434_2435insTCATAG	ENSP00000390987.2:p.Arg811_Asp812insValIle
ENST00000512959.1:n.499_500insTCATAG
NM_000222.2:c.2446_2447insTCATAG , LRG_307t1:c.2446_2447insTCATAG	NP_000213.1:p.Arg815_Asp816insValIle
NM_001093772.1:c.2434_2435insTCATAG	NP_001087241.1:p.Arg811_Asp812insValIle
XM_005265740.1:c.2449_2450insTCATAG	XP_005265797.1:p.Arg816_Asp817insValIle
XM_005265741.1:c.2446_2447insTCATAG	XP_005265798.1:p.Arg815_Asp816insValIle
XM_005265742.1:c.2437_2438insTCATAG	XP_005265799.1:p.Arg812_Asp813insValIle
XM_005265742.3:c.2437_2438insTCATAG	XP_005265799.1:p.Arg812_Asp813insValIle
XM_017008178.1:c.2443_2444insTCATAG	XP_016863667.1:p.Arg814_Asp815insValIle
XM_017008179.1:c.2434_2435insTCATAG	XP_016863668.1:p.Arg811_Asp812insValIle
XM_017008180.1:c.2431_2432insTCATAG	XP_016863669.1:p.Arg810_Asp811insValIle
NM_000222.3:c.2446_2447insTCATAG MANE Select	NP_000213.1:p.Arg815_Asp816insValIle
NM_001093772.2:c.2434_2435insTCATAG	NP_001087241.1:p.Arg811_Asp812insValIle
NM_001385284.1:c.2449_2450insTCATAG	NP_001372213.1:p.Arg816_Asp817insValIle
NM_001385285.1:c.2443_2444insTCATAG	NP_001372214.1:p.Arg814_Asp815insValIle
NM_001385286.1:c.2431_2432insTCATAG	NP_001372215.1:p.Arg810_Asp811insValIle
NM_001385288.1:c.2437_2438insTCATAG	NP_001372217.1:p.Arg812_Asp813insValIle
NM_001385290.1:c.2446_2447insTCATAG	NP_001372219.1:p.Arg815_Asp816insValIle
NM_001385292.1:c.2434_2435insTCATAG	NP_001372221.1:p.Arg811_Asp812insValIle