Canonical Allele Identifier: CA1458744590
Gene: KIT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54733494_54733495delinsTA , CM000666.2:g.54733494_54733495delinsTA GRCh38
NC_000004.11:g.55599660_55599661delinsTA , CM000666.1:g.55599660_55599661delinsTA GRCh37
NC_000004.10:g.55294417_55294418delinsTA NCBI36
NG_007456.1:g.80500_80501delinsTA , LRG_307:g.80500_80501delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.2472+302_2472+303delinsTA ENSP00000390987.3:n.2472+302_2472+303delinsTA
ENST00000685269.1:n.2562+302_2562+303delinsTA
ENST00000686011.1:c.2469+302_2469+303delinsTA ENSP00000509704.1:n.2469+302_2469+303delinsTA
ENST00000687109.1:c.2487+302_2487+303delinsTA ENSP00000509371.1:n.2487+302_2487+303delinsTA
ENST00000687208.1:n.2896+302_2896+303delinsTA
ENST00000687246.1:c.2349+1496_2349+1497delinsTA ENSP00000509114.1:n.2349+1496_2349+1497delinsTA
ENST00000687265.1:n.2642+302_2642+303delinsTA
ENST00000687295.1:c.2472+302_2472+303delinsTA ENSP00000509450.1:n.2472+302_2472+303delinsTA
ENST00000688060.1:n.281+302_281+303delinsTA
ENST00000688704.1:n.1798_1799delinsTA
ENST00000689832.1:c.2484+302_2484+303delinsTA ENSP00000509084.1:n.2484+302_2484+303delinsTA
ENST00000689994.1:c.1974+302_1974+303delinsTA ENSP00000509156.1:n.1974+302_1974+303delinsTA
ENST00000690543.1:c.2475+302_2475+303delinsTA ENSP00000508831.1:n.2475+302_2475+303delinsTA
ENST00000690917.1:n.2702+302_2702+303delinsTA
ENST00000691361.1:n.1394+302_1394+303delinsTA
ENST00000692783.1:c.2481+302_2481+303delinsTA ENSP00000508733.1:n.2481+302_2481+303delinsTA
ENST00000692991.1:n.2581+302_2581+303delinsTA
ENST00000288135.6:c.2484+302_2484+303delinsTA MANE Select ENSP00000288135.6:n.2484+302_2484+303delinsTA
ENST00000288135.5:c.2484+302_2484+303delinsTA ENSP00000288135.5:n.2484+302_2484+303delinsTA
ENST00000412167.6:c.2472+302_2472+303delinsTA ENSP00000390987.2:n.2472+302_2472+303delinsTA
NM_000222.2:c.2484+302_2484+303delinsTA , LRG_307t1:c.2484+302_2484+303delinsTA NP_000213.1:n.2484+302_2484+303delinsTA
NM_001093772.1:c.2472+302_2472+303delinsTA NP_001087241.1:n.2472+302_2472+303delinsTA
XM_005265740.1:c.2487+302_2487+303delinsTA XP_005265797.1:n.2487+302_2487+303delinsTA
XM_005265741.1:c.2484+302_2484+303delinsTA XP_005265798.1:n.2484+302_2484+303delinsTA
XM_005265742.1:c.2475+302_2475+303delinsTA XP_005265799.1:n.2475+302_2475+303delinsTA
XM_005265742.3:c.2475+302_2475+303delinsTA XP_005265799.1:n.2475+302_2475+303delinsTA
XM_017008178.1:c.2481+302_2481+303delinsTA XP_016863667.1:n.2481+302_2481+303delinsTA
XM_017008179.1:c.2472+302_2472+303delinsTA XP_016863668.1:n.2472+302_2472+303delinsTA
XM_017008180.1:c.2469+302_2469+303delinsTA XP_016863669.1:n.2469+302_2469+303delinsTA
NM_000222.3:c.2484+302_2484+303delinsTA MANE Select NP_000213.1:n.2484+302_2484+303delinsTA
NM_001093772.2:c.2472+302_2472+303delinsTA NP_001087241.1:n.2472+302_2472+303delinsTA
NM_001385284.1:c.2487+302_2487+303delinsTA NP_001372213.1:n.2487+302_2487+303delinsTA
NM_001385285.1:c.2481+302_2481+303delinsTA NP_001372214.1:n.2481+302_2481+303delinsTA
NM_001385286.1:c.2469+302_2469+303delinsTA NP_001372215.1:n.2469+302_2469+303delinsTA
NM_001385288.1:c.2475+302_2475+303delinsTA NP_001372217.1:n.2475+302_2475+303delinsTA
NM_001385290.1:c.2484+302_2484+303delinsTA NP_001372219.1:n.2484+302_2484+303delinsTA
NM_001385292.1:c.2472+302_2472+303delinsTA NP_001372221.1:n.2472+302_2472+303delinsTA