Canonical Allele Identifier: CA2850447376
Gene: KIT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54733155_54733156delinsTT , CM000666.2:g.54733155_54733156delinsTT GRCh38
NC_000004.11:g.55599321_55599322delinsTT , CM000666.1:g.55599321_55599322delinsTT GRCh37
NC_000004.10:g.55294078_55294079delinsTT NCBI36
NG_007456.1:g.80161_80162delinsTT , LRG_307:g.80161_80162delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.2435_2436delinsTT ENSP00000390987.3:p.Asp812Val
ENST00000685269.1:n.2525_2526delinsTT
ENST00000686011.1:c.2432_2433delinsTT ENSP00000509704.1:p.Asp811Val
ENST00000687109.1:c.2450_2451delinsTT ENSP00000509371.1:p.Asp817Val
ENST00000687208.1:n.2859_2860delinsTT
ENST00000687246.1:c.2349+1157_2349+1158delinsTT ENSP00000509114.1:n.2349+1157_2349+1158delinsTT
ENST00000687265.1:n.2605_2606delinsTT
ENST00000687295.1:c.2435_2436delinsTT ENSP00000509450.1:p.Asp812Val
ENST00000688060.1:n.244_245delinsTT
ENST00000688704.1:n.1459_1460delinsTT
ENST00000689832.1:c.2447_2448delinsTT ENSP00000509084.1:p.Asp816Val
ENST00000689994.1:c.1937_1938delinsTT ENSP00000509156.1:p.Asp646Val
ENST00000690543.1:c.2438_2439delinsTT ENSP00000508831.1:p.Asp813Val
ENST00000690917.1:n.2665_2666delinsTT
ENST00000691361.1:n.1357_1358delinsTT
ENST00000692783.1:c.2444_2445delinsTT ENSP00000508733.1:p.Asp815Val
ENST00000692991.1:n.2544_2545delinsTT
ENST00000288135.6:c.2447_2448delinsTT MANE Select ENSP00000288135.6:p.Asp816Val
ENST00000288135.5:c.2447_2448delinsTT ENSP00000288135.5:p.Asp816Val
ENST00000412167.6:c.2435_2436delinsTT ENSP00000390987.2:p.Asp812Val
ENST00000512959.1:n.500_501delinsTT
NM_000222.2:c.2447_2448delinsTT , LRG_307t1:c.2447_2448delinsTT NP_000213.1:p.Asp816Val
NM_001093772.1:c.2435_2436delinsTT NP_001087241.1:p.Asp812Val
XM_005265740.1:c.2450_2451delinsTT XP_005265797.1:p.Asp817Val
XM_005265741.1:c.2447_2448delinsTT XP_005265798.1:p.Asp816Val
XM_005265742.1:c.2438_2439delinsTT XP_005265799.1:p.Asp813Val
XM_005265742.3:c.2438_2439delinsTT XP_005265799.1:p.Asp813Val
XM_017008178.1:c.2444_2445delinsTT XP_016863667.1:p.Asp815Val
XM_017008179.1:c.2435_2436delinsTT XP_016863668.1:p.Asp812Val
XM_017008180.1:c.2432_2433delinsTT XP_016863669.1:p.Asp811Val
NM_000222.3:c.2447_2448delinsTT MANE Select NP_000213.1:p.Asp816Val
NM_001093772.2:c.2435_2436delinsTT NP_001087241.1:p.Asp812Val
NM_001385284.1:c.2450_2451delinsTT NP_001372213.1:p.Asp817Val
NM_001385285.1:c.2444_2445delinsTT NP_001372214.1:p.Asp815Val
NM_001385286.1:c.2432_2433delinsTT NP_001372215.1:p.Asp811Val
NM_001385288.1:c.2438_2439delinsTT NP_001372217.1:p.Asp813Val
NM_001385290.1:c.2447_2448delinsTT NP_001372219.1:p.Asp816Val
NM_001385292.1:c.2435_2436delinsTT NP_001372221.1:p.Asp812Val