Canonical Allele Identifier: CA2761715260
Gene: KIT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54736633_54736634insCCCAACAC , CM000666.2:g.54736633_54736634insCCCAACAC GRCh38
NC_000004.11:g.55602799_55602800insCCCAACAC , CM000666.1:g.55602799_55602800insCCCAACAC GRCh37
NC_000004.10:g.55297556_55297557insCCCAACAC NCBI36
NG_007456.1:g.83639_83640insCCCAACAC , LRG_307:g.83639_83640insCCCAACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.2584+24_2584+25insCCCAACAC ENSP00000390987.3:n.2584+24_2584+25insCCCAACAC
ENST00000684818.1:n.1288+24_1288+25insCCCAACAC
ENST00000685269.1:n.2674+24_2674+25insCCCAACAC
ENST00000686011.1:c.2581+24_2581+25insCCCAACAC ENSP00000509704.1:n.2581+24_2581+25insCCCAACAC
ENST00000687109.1:c.2599+24_2599+25insCCCAACAC ENSP00000509371.1:n.2599+24_2599+25insCCCAACAC
ENST00000687208.1:n.3008+24_3008+25insCCCAACAC
ENST00000687246.1:c.2461+24_2461+25insCCCAACAC ENSP00000509114.1:n.2461+24_2461+25insCCCAACAC
ENST00000687265.1:n.2754+24_2754+25insCCCAACAC
ENST00000687295.1:c.2584+24_2584+25insCCCAACAC ENSP00000509450.1:n.2584+24_2584+25insCCCAACAC
ENST00000688060.1:n.393+24_393+25insCCCAACAC
ENST00000689832.1:c.2596+24_2596+25insCCCAACAC ENSP00000509084.1:n.2596+24_2596+25insCCCAACAC
ENST00000689994.1:c.2086+24_2086+25insCCCAACAC ENSP00000509156.1:n.2086+24_2086+25insCCCAACAC
ENST00000690543.1:c.2587+24_2587+25insCCCAACAC ENSP00000508831.1:n.2587+24_2587+25insCCCAACAC
ENST00000690917.1:n.2814+24_2814+25insCCCAACAC
ENST00000691361.1:n.1506+24_1506+25insCCCAACAC
ENST00000692301.1:n.1288+24_1288+25insCCCAACAC
ENST00000692783.1:c.2593+24_2593+25insCCCAACAC ENSP00000508733.1:n.2593+24_2593+25insCCCAACAC
ENST00000692991.1:n.2693+24_2693+25insCCCAACAC
ENST00000288135.6:c.2596+24_2596+25insCCCAACAC MANE Select ENSP00000288135.6:n.2596+24_2596+25insCCCAACAC
ENST00000288135.5:c.2596+24_2596+25insCCCAACAC ENSP00000288135.5:n.2596+24_2596+25insCCCAACAC
ENST00000412167.6:c.2584+24_2584+25insCCCAACAC ENSP00000390987.2:n.2584+24_2584+25insCCCAACAC
NM_000222.2:c.2596+24_2596+25insCCCAACAC , LRG_307t1:c.2596+24_2596+25insCCCAACAC NP_000213.1:n.2596+24_2596+25insCCCAACAC
NM_001093772.1:c.2584+24_2584+25insCCCAACAC NP_001087241.1:n.2584+24_2584+25insCCCAACAC
XM_005265740.1:c.2599+24_2599+25insCCCAACAC XP_005265797.1:n.2599+24_2599+25insCCCAACAC
XM_005265741.1:c.2596+24_2596+25insCCCAACAC XP_005265798.1:n.2596+24_2596+25insCCCAACAC
XM_005265742.1:c.2587+24_2587+25insCCCAACAC XP_005265799.1:n.2587+24_2587+25insCCCAACAC
XM_005265742.3:c.2587+24_2587+25insCCCAACAC XP_005265799.1:n.2587+24_2587+25insCCCAACAC
XM_017008178.1:c.2593+24_2593+25insCCCAACAC XP_016863667.1:n.2593+24_2593+25insCCCAACAC
XM_017008179.1:c.2584+24_2584+25insCCCAACAC XP_016863668.1:n.2584+24_2584+25insCCCAACAC
XM_017008180.1:c.2581+24_2581+25insCCCAACAC XP_016863669.1:n.2581+24_2581+25insCCCAACAC
NM_000222.3:c.2596+24_2596+25insCCCAACAC MANE Select NP_000213.1:n.2596+24_2596+25insCCCAACAC
NM_001093772.2:c.2584+24_2584+25insCCCAACAC NP_001087241.1:n.2584+24_2584+25insCCCAACAC
NM_001385284.1:c.2599+24_2599+25insCCCAACAC NP_001372213.1:n.2599+24_2599+25insCCCAACAC
NM_001385285.1:c.2593+24_2593+25insCCCAACAC NP_001372214.1:n.2593+24_2593+25insCCCAACAC
NM_001385286.1:c.2581+24_2581+25insCCCAACAC NP_001372215.1:n.2581+24_2581+25insCCCAACAC
NM_001385288.1:c.2587+24_2587+25insCCCAACAC NP_001372217.1:n.2587+24_2587+25insCCCAACAC
NM_001385290.1:c.2596+24_2596+25insCCCAACAC NP_001372219.1:n.2596+24_2596+25insCCCAACAC
NM_001385292.1:c.2584+24_2584+25insCCCAACAC NP_001372221.1:n.2584+24_2584+25insCCCAACAC