Canonical Allele Identifier: CA645516777

Gene: KIT

Linked Data

• COSMIC: COSM36310

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727428_54727454del , CM000666.2:g.54727428_54727454del	GRCh38
NC_000004.11:g.55593594_55593620del , CM000666.1:g.55593594_55593620del	GRCh37
NC_000004.10:g.55288351_55288377del	NCBI36
NG_007456.1:g.74434_74460del , LRG_307:g.74434_74460del

Transcript Alleles

HGVS	Amino-acid change
ENST00000412167.7:c.1651_1677del	ENSP00000390987.3:p.Glu551_Glu559del
ENST00000685269.1:n.1738_1764del
ENST00000686011.1:c.1648_1674del	ENSP00000509704.1:p.Glu550_Glu558del
ENST00000687109.1:c.1663_1689del	ENSP00000509371.1:p.Glu555_Glu563del
ENST00000687208.1:n.2075_2101del
ENST00000687246.1:c.1648_1674del	ENSP00000509114.1:p.Glu550_Glu558del
ENST00000687265.1:n.1818_1844del
ENST00000687295.1:c.1648_1674del	ENSP00000509450.1:p.Glu550_Glu558del
ENST00000689832.1:c.1663_1689del	ENSP00000509084.1:p.Glu555_Glu563del
ENST00000689994.1:c.1150_1176del	ENSP00000509156.1:p.Glu384_Glu392del
ENST00000690543.1:c.1651_1677del	ENSP00000508831.1:p.Glu551_Glu559del
ENST00000690917.1:n.1878_1904del
ENST00000691361.1:n.570_596del
ENST00000692783.1:c.1660_1686del	ENSP00000508733.1:p.Glu554_Glu562del
ENST00000692991.1:n.1757_1783del
ENST00000288135.6:c.1660_1686del MANE Select	ENSP00000288135.6:p.Glu554_Glu562del
ENST00000288135.5:c.1660_1686del	ENSP00000288135.5:p.Glu554_Glu562del
ENST00000412167.6:c.1648_1674del	ENSP00000390987.2:p.Glu550_Glu558del
NM_000222.2:c.1660_1686del , LRG_307t1:c.1660_1686del	NP_000213.1:p.Glu554_Glu562del
NM_001093772.1:c.1648_1674del	NP_001087241.1:p.Glu550_Glu558del
XM_005265740.1:c.1663_1689del	XP_005265797.1:p.Glu555_Glu563del
XM_005265741.1:c.1663_1689del	XP_005265798.1:p.Glu555_Glu563del
XM_005265742.1:c.1651_1677del	XP_005265799.1:p.Glu551_Glu559del
XM_005265742.3:c.1651_1677del	XP_005265799.1:p.Glu551_Glu559del
XM_017008178.1:c.1660_1686del	XP_016863667.1:p.Glu554_Glu562del
XM_017008179.1:c.1651_1677del	XP_016863668.1:p.Glu551_Glu559del
XM_017008180.1:c.1648_1674del	XP_016863669.1:p.Glu550_Glu558del
NM_000222.3:c.1660_1686del MANE Select	NP_000213.1:p.Glu554_Glu562del
NM_001093772.2:c.1648_1674del	NP_001087241.1:p.Glu550_Glu558del
NM_001385284.1:c.1663_1689del	NP_001372213.1:p.Glu555_Glu563del
NM_001385285.1:c.1660_1686del	NP_001372214.1:p.Glu554_Glu562del
NM_001385286.1:c.1648_1674del	NP_001372215.1:p.Glu550_Glu558del
NM_001385288.1:c.1651_1677del	NP_001372217.1:p.Glu551_Glu559del
NM_001385290.1:c.1663_1689del	NP_001372219.1:p.Glu555_Glu563del
NM_001385292.1:c.1651_1677del	NP_001372221.1:p.Glu551_Glu559del