Canonical Allele Identifier: CA1458739321

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727790_54727791delinsTC , CM000666.2:g.54727790_54727791delinsTC	GRCh38
NC_000004.11:g.55593956_55593957delinsTC , CM000666.1:g.55593956_55593957delinsTC	GRCh37
NC_000004.10:g.55288713_55288714delinsTC	NCBI36
NG_007456.1:g.74796_74797delinsTC , LRG_307:g.74796_74797delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1766-33_1766-32delinsTC	ENSP00000390987.3:n.1766-33_1766-32delinsTC
ENST00000685269.1:n.1853-33_1853-32delinsTC
ENST00000686011.1:c.1763-33_1763-32delinsTC	ENSP00000509704.1:n.1763-33_1763-32delinsTC
ENST00000687109.1:c.1778-33_1778-32delinsTC	ENSP00000509371.1:n.1778-33_1778-32delinsTC
ENST00000687208.1:n.2190-33_2190-32delinsTC
ENST00000687246.1:c.1763-33_1763-32delinsTC	ENSP00000509114.1:n.1763-33_1763-32delinsTC
ENST00000687265.1:n.1933-33_1933-32delinsTC
ENST00000687295.1:c.1763-33_1763-32delinsTC	ENSP00000509450.1:n.1763-33_1763-32delinsTC
ENST00000689832.1:c.1778-33_1778-32delinsTC	ENSP00000509084.1:n.1778-33_1778-32delinsTC
ENST00000689994.1:c.1265-33_1265-32delinsTC	ENSP00000509156.1:n.1265-33_1265-32delinsTC
ENST00000690543.1:c.1766-33_1766-32delinsTC	ENSP00000508831.1:n.1766-33_1766-32delinsTC
ENST00000690917.1:n.1993-33_1993-32delinsTC
ENST00000691361.1:n.685-33_685-32delinsTC
ENST00000692783.1:c.1775-33_1775-32delinsTC	ENSP00000508733.1:n.1775-33_1775-32delinsTC
ENST00000692991.1:n.1872-33_1872-32delinsTC
ENST00000288135.6:c.1775-33_1775-32delinsTC MANE Select	ENSP00000288135.6:n.1775-33_1775-32delinsTC
ENST00000288135.5:c.1775-33_1775-32delinsTC	ENSP00000288135.5:n.1775-33_1775-32delinsTC
ENST00000412167.6:c.1763-33_1763-32delinsTC	ENSP00000390987.2:n.1763-33_1763-32delinsTC
NM_000222.2:c.1775-33_1775-32delinsTC , LRG_307t1:c.1775-33_1775-32delinsTC	NP_000213.1:n.1775-33_1775-32delinsTC
NM_001093772.1:c.1763-33_1763-32delinsTC	NP_001087241.1:n.1763-33_1763-32delinsTC
XM_005265740.1:c.1778-33_1778-32delinsTC	XP_005265797.1:n.1778-33_1778-32delinsTC
XM_005265741.1:c.1778-33_1778-32delinsTC	XP_005265798.1:n.1778-33_1778-32delinsTC
XM_005265742.1:c.1766-33_1766-32delinsTC	XP_005265799.1:n.1766-33_1766-32delinsTC
XM_005265742.3:c.1766-33_1766-32delinsTC	XP_005265799.1:n.1766-33_1766-32delinsTC
XM_017008178.1:c.1775-33_1775-32delinsTC	XP_016863667.1:n.1775-33_1775-32delinsTC
XM_017008179.1:c.1766-33_1766-32delinsTC	XP_016863668.1:n.1766-33_1766-32delinsTC
XM_017008180.1:c.1763-33_1763-32delinsTC	XP_016863669.1:n.1763-33_1763-32delinsTC
NM_000222.3:c.1775-33_1775-32delinsTC MANE Select	NP_000213.1:n.1775-33_1775-32delinsTC
NM_001093772.2:c.1763-33_1763-32delinsTC	NP_001087241.1:n.1763-33_1763-32delinsTC
NM_001385284.1:c.1778-33_1778-32delinsTC	NP_001372213.1:n.1778-33_1778-32delinsTC
NM_001385285.1:c.1775-33_1775-32delinsTC	NP_001372214.1:n.1775-33_1775-32delinsTC
NM_001385286.1:c.1763-33_1763-32delinsTC	NP_001372215.1:n.1763-33_1763-32delinsTC
NM_001385288.1:c.1766-33_1766-32delinsTC	NP_001372217.1:n.1766-33_1766-32delinsTC
NM_001385290.1:c.1778-33_1778-32delinsTC	NP_001372219.1:n.1778-33_1778-32delinsTC
NM_001385292.1:c.1766-33_1766-32delinsTC	NP_001372221.1:n.1766-33_1766-32delinsTC