Canonical Allele Identifier: CA645516783

Gene: KIT

Linked Data

• COSMIC: COSM1198 ; COSM30549

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727433_54727447del , CM000666.2:g.54727433_54727447del	GRCh38
NC_000004.11:g.55593599_55593613del , CM000666.1:g.55593599_55593613del	GRCh37
NC_000004.10:g.55288356_55288370del	NCBI36
NG_007456.1:g.74439_74453del , LRG_307:g.74439_74453del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1656_1670del	ENSP00000390987.3:p.Gln553_Val557del
ENST00000685269.1:n.1743_1757del
ENST00000686011.1:c.1653_1667del	ENSP00000509704.1:p.Gln552_Val556del
ENST00000687109.1:c.1668_1682del	ENSP00000509371.1:p.Gln557_Val561del
ENST00000687208.1:n.2080_2094del
ENST00000687246.1:c.1653_1667del	ENSP00000509114.1:p.Gln552_Val556del
ENST00000687265.1:n.1823_1837del
ENST00000687295.1:c.1653_1667del	ENSP00000509450.1:p.Gln552_Val556del
ENST00000689832.1:c.1668_1682del	ENSP00000509084.1:p.Gln557_Val561del
ENST00000689994.1:c.1155_1169del	ENSP00000509156.1:p.Gln386_Val390del
ENST00000690543.1:c.1656_1670del	ENSP00000508831.1:p.Gln553_Val557del
ENST00000690917.1:n.1883_1897del
ENST00000691361.1:n.575_589del
ENST00000692783.1:c.1665_1679del	ENSP00000508733.1:p.Gln556_Val560del
ENST00000692991.1:n.1762_1776del
ENST00000288135.6:c.1665_1679del MANE Select	ENSP00000288135.6:p.Gln556_Val560del
ENST00000288135.5:c.1665_1679del	ENSP00000288135.5:p.Gln556_Val560del
ENST00000412167.6:c.1653_1667del	ENSP00000390987.2:p.Gln552_Val556del
NM_000222.2:c.1665_1679del , LRG_307t1:c.1665_1679del	NP_000213.1:p.Gln556_Val560del
NM_001093772.1:c.1653_1667del	NP_001087241.1:p.Gln552_Val556del
XM_005265740.1:c.1668_1682del	XP_005265797.1:p.Gln557_Val561del
XM_005265741.1:c.1668_1682del	XP_005265798.1:p.Gln557_Val561del
XM_005265742.1:c.1656_1670del	XP_005265799.1:p.Gln553_Val557del
XM_005265742.3:c.1656_1670del	XP_005265799.1:p.Gln553_Val557del
XM_017008178.1:c.1665_1679del	XP_016863667.1:p.Gln556_Val560del
XM_017008179.1:c.1656_1670del	XP_016863668.1:p.Gln553_Val557del
XM_017008180.1:c.1653_1667del	XP_016863669.1:p.Gln552_Val556del
NM_000222.3:c.1665_1679del MANE Select	NP_000213.1:p.Gln556_Val560del
NM_001093772.2:c.1653_1667del	NP_001087241.1:p.Gln552_Val556del
NM_001385284.1:c.1668_1682del	NP_001372213.1:p.Gln557_Val561del
NM_001385285.1:c.1665_1679del	NP_001372214.1:p.Gln556_Val560del
NM_001385286.1:c.1653_1667del	NP_001372215.1:p.Gln552_Val556del
NM_001385288.1:c.1656_1670del	NP_001372217.1:p.Gln553_Val557del
NM_001385290.1:c.1668_1682del	NP_001372219.1:p.Gln557_Val561del
NM_001385292.1:c.1656_1670del	NP_001372221.1:p.Gln553_Val557del