Canonical Allele Identifier: CA1458743999

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54732948_54732954delinsTTAAAAC , CM000666.2:g.54732948_54732954delinsTTAAAAC	GRCh38
NC_000004.11:g.55599114_55599120delinsTTAAAAC , CM000666.1:g.55599114_55599120delinsTTAAAAC	GRCh37
NC_000004.10:g.55293871_55293877delinsTTAAAAC	NCBI36
NG_007456.1:g.79954_79960delinsTTAAAAC , LRG_307:g.79954_79960delinsTTAAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.2350-122_2350-116delinsTTAAAAC	ENSP00000390987.3:n.2350-122_2350-116delinsTTAAAAC
ENST00000685269.1:n.2440-122_2440-116delinsTTAAAAC
ENST00000686011.1:c.2347-122_2347-116delinsTTAAAAC	ENSP00000509704.1:n.2347-122_2347-116delinsTTAAAAC
ENST00000687109.1:c.2365-122_2365-116delinsTTAAAAC	ENSP00000509371.1:n.2365-122_2365-116delinsTTAAAAC
ENST00000687208.1:n.2774-122_2774-116delinsTTAAAAC
ENST00000687246.1:c.2349+950_2349+956delinsTTAAAAC	ENSP00000509114.1:n.2349+950_2349+956delinsTTAAAAC
ENST00000687265.1:n.2520-122_2520-116delinsTTAAAAC
ENST00000687295.1:c.2350-122_2350-116delinsTTAAAAC	ENSP00000509450.1:n.2350-122_2350-116delinsTTAAAAC
ENST00000688060.1:n.159-122_159-116delinsTTAAAAC
ENST00000688704.1:n.1252_1258delinsTTAAAAC
ENST00000689832.1:c.2362-122_2362-116delinsTTAAAAC	ENSP00000509084.1:n.2362-122_2362-116delinsTTAAAAC
ENST00000689994.1:c.1852-122_1852-116delinsTTAAAAC	ENSP00000509156.1:n.1852-122_1852-116delinsTTAAAAC
ENST00000690543.1:c.2353-122_2353-116delinsTTAAAAC	ENSP00000508831.1:n.2353-122_2353-116delinsTTAAAAC
ENST00000690917.1:n.2580-122_2580-116delinsTTAAAAC
ENST00000691361.1:n.1272-122_1272-116delinsTTAAAAC
ENST00000692783.1:c.2359-122_2359-116delinsTTAAAAC	ENSP00000508733.1:n.2359-122_2359-116delinsTTAAAAC
ENST00000692991.1:n.2459-122_2459-116delinsTTAAAAC
ENST00000288135.6:c.2362-122_2362-116delinsTTAAAAC MANE Select	ENSP00000288135.6:n.2362-122_2362-116delinsTTAAAAC
ENST00000288135.5:c.2362-122_2362-116delinsTTAAAAC	ENSP00000288135.5:n.2362-122_2362-116delinsTTAAAAC
ENST00000412167.6:c.2350-122_2350-116delinsTTAAAAC	ENSP00000390987.2:n.2350-122_2350-116delinsTTAAAAC
ENST00000512959.1:n.415-122_415-116delinsTTAAAAC
NM_000222.2:c.2362-122_2362-116delinsTTAAAAC , LRG_307t1:c.2362-122_2362-116delinsTTAAAAC	NP_000213.1:n.2362-122_2362-116delinsTTAAAAC
NM_001093772.1:c.2350-122_2350-116delinsTTAAAAC	NP_001087241.1:n.2350-122_2350-116delinsTTAAAAC
XM_005265740.1:c.2365-122_2365-116delinsTTAAAAC	XP_005265797.1:n.2365-122_2365-116delinsTTAAAAC
XM_005265741.1:c.2362-122_2362-116delinsTTAAAAC	XP_005265798.1:n.2362-122_2362-116delinsTTAAAAC
XM_005265742.1:c.2353-122_2353-116delinsTTAAAAC	XP_005265799.1:n.2353-122_2353-116delinsTTAAAAC
XM_005265742.3:c.2353-122_2353-116delinsTTAAAAC	XP_005265799.1:n.2353-122_2353-116delinsTTAAAAC
XM_017008178.1:c.2359-122_2359-116delinsTTAAAAC	XP_016863667.1:n.2359-122_2359-116delinsTTAAAAC
XM_017008179.1:c.2350-122_2350-116delinsTTAAAAC	XP_016863668.1:n.2350-122_2350-116delinsTTAAAAC
XM_017008180.1:c.2347-122_2347-116delinsTTAAAAC	XP_016863669.1:n.2347-122_2347-116delinsTTAAAAC
NM_000222.3:c.2362-122_2362-116delinsTTAAAAC MANE Select	NP_000213.1:n.2362-122_2362-116delinsTTAAAAC
NM_001093772.2:c.2350-122_2350-116delinsTTAAAAC	NP_001087241.1:n.2350-122_2350-116delinsTTAAAAC
NM_001385284.1:c.2365-122_2365-116delinsTTAAAAC	NP_001372213.1:n.2365-122_2365-116delinsTTAAAAC
NM_001385285.1:c.2359-122_2359-116delinsTTAAAAC	NP_001372214.1:n.2359-122_2359-116delinsTTAAAAC
NM_001385286.1:c.2347-122_2347-116delinsTTAAAAC	NP_001372215.1:n.2347-122_2347-116delinsTTAAAAC
NM_001385288.1:c.2353-122_2353-116delinsTTAAAAC	NP_001372217.1:n.2353-122_2353-116delinsTTAAAAC
NM_001385290.1:c.2362-122_2362-116delinsTTAAAAC	NP_001372219.1:n.2362-122_2362-116delinsTTAAAAC
NM_001385292.1:c.2350-122_2350-116delinsTTAAAAC	NP_001372221.1:n.2350-122_2350-116delinsTTAAAAC