Canonical Allele Identifier: CA645516948
Gene: KIT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54733154_54733155delinsTT , CM000666.2:g.54733154_54733155delinsTT GRCh38
NC_000004.11:g.55599320_55599321delinsTT , CM000666.1:g.55599320_55599321delinsTT GRCh37
NC_000004.10:g.55294077_55294078delinsTT NCBI36
NG_007456.1:g.80160_80161delinsTT , LRG_307:g.80160_80161delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.2434_2435delinsTT ENSP00000390987.3:p.Asp812Phe
ENST00000685269.1:n.2524_2525delinsTT
ENST00000686011.1:c.2431_2432delinsTT ENSP00000509704.1:p.Asp811Phe
ENST00000687109.1:c.2449_2450delinsTT ENSP00000509371.1:p.Asp817Phe
ENST00000687208.1:n.2858_2859delinsTT
ENST00000687246.1:c.2349+1156_2349+1157delinsTT ENSP00000509114.1:n.2349+1156_2349+1157delinsTT
ENST00000687265.1:n.2604_2605delinsTT
ENST00000687295.1:c.2434_2435delinsTT ENSP00000509450.1:p.Asp812Phe
ENST00000688060.1:n.243_244delinsTT
ENST00000688704.1:n.1458_1459delinsTT
ENST00000689832.1:c.2446_2447delinsTT ENSP00000509084.1:p.Asp816Phe
ENST00000689994.1:c.1936_1937delinsTT ENSP00000509156.1:p.Asp646Phe
ENST00000690543.1:c.2437_2438delinsTT ENSP00000508831.1:p.Asp813Phe
ENST00000690917.1:n.2664_2665delinsTT
ENST00000691361.1:n.1356_1357delinsTT
ENST00000692783.1:c.2443_2444delinsTT ENSP00000508733.1:p.Asp815Phe
ENST00000692991.1:n.2543_2544delinsTT
ENST00000288135.6:c.2446_2447delinsTT MANE Select ENSP00000288135.6:p.Asp816Phe
ENST00000288135.5:c.2446_2447delinsTT ENSP00000288135.5:p.Asp816Phe
ENST00000412167.6:c.2434_2435delinsTT ENSP00000390987.2:p.Asp812Phe
ENST00000512959.1:n.499_500delinsTT
NM_000222.2:c.2446_2447delinsTT , LRG_307t1:c.2446_2447delinsTT NP_000213.1:p.Asp816Phe
NM_001093772.1:c.2434_2435delinsTT NP_001087241.1:p.Asp812Phe
XM_005265740.1:c.2449_2450delinsTT XP_005265797.1:p.Asp817Phe
XM_005265741.1:c.2446_2447delinsTT XP_005265798.1:p.Asp816Phe
XM_005265742.1:c.2437_2438delinsTT XP_005265799.1:p.Asp813Phe
XM_005265742.3:c.2437_2438delinsTT XP_005265799.1:p.Asp813Phe
XM_017008178.1:c.2443_2444delinsTT XP_016863667.1:p.Asp815Phe
XM_017008179.1:c.2434_2435delinsTT XP_016863668.1:p.Asp812Phe
XM_017008180.1:c.2431_2432delinsTT XP_016863669.1:p.Asp811Phe
NM_000222.3:c.2446_2447delinsTT MANE Select NP_000213.1:p.Asp816Phe
NM_001093772.2:c.2434_2435delinsTT NP_001087241.1:p.Asp812Phe
NM_001385284.1:c.2449_2450delinsTT NP_001372213.1:p.Asp817Phe
NM_001385285.1:c.2443_2444delinsTT NP_001372214.1:p.Asp815Phe
NM_001385286.1:c.2431_2432delinsTT NP_001372215.1:p.Asp811Phe
NM_001385288.1:c.2437_2438delinsTT NP_001372217.1:p.Asp813Phe
NM_001385290.1:c.2446_2447delinsTT NP_001372219.1:p.Asp816Phe
NM_001385292.1:c.2434_2435delinsTT NP_001372221.1:p.Asp812Phe