Canonical Allele Identifier: CA645516814

Gene: KIT

Linked Data

• COSMIC: COSM27902

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727436_54727447delinsCAACCTTCCACTGTA , CM000666.2:g.54727436_54727447delinsCAACCTTCCACTGTA	GRCh38
NC_000004.11:g.55593602_55593613delinsCAACCTTCCACTGTA , CM000666.1:g.55593602_55593613delinsCAACCTTCCACTGTA	GRCh37
NC_000004.10:g.55288359_55288370delinsCAACCTTCCACTGTA	NCBI36
NG_007456.1:g.74442_74453delinsCAACCTTCCACTGTA , LRG_307:g.74442_74453delinsCAACCTTCCACTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1659_1670delinsCAACCTTCCACTGTA	ENSP00000390987.3:p.Gln553_Val557delinsHisAsnLeuProLeuTyr
ENST00000685269.1:n.1746_1757delinsCAACCTTCCACTGTA
ENST00000686011.1:c.1656_1667delinsCAACCTTCCACTGTA	ENSP00000509704.1:p.Gln552_Val556delinsHisAsnLeuProLeuTyr
ENST00000687109.1:c.1671_1682delinsCAACCTTCCACTGTA	ENSP00000509371.1:p.Gln557_Val561delinsHisAsnLeuProLeuTyr
ENST00000687208.1:n.2083_2094delinsCAACCTTCCACTGTA
ENST00000687246.1:c.1656_1667delinsCAACCTTCCACTGTA	ENSP00000509114.1:p.Gln552_Val556delinsHisAsnLeuProLeuTyr
ENST00000687265.1:n.1826_1837delinsCAACCTTCCACTGTA
ENST00000687295.1:c.1656_1667delinsCAACCTTCCACTGTA	ENSP00000509450.1:p.Gln552_Val556delinsHisAsnLeuProLeuTyr
ENST00000689832.1:c.1671_1682delinsCAACCTTCCACTGTA	ENSP00000509084.1:p.Gln557_Val561delinsHisAsnLeuProLeuTyr
ENST00000689994.1:c.1158_1169delinsCAACCTTCCACTGTA	ENSP00000509156.1:p.Gln386_Val390delinsHisAsnLeuProLeuTyr
ENST00000690543.1:c.1659_1670delinsCAACCTTCCACTGTA	ENSP00000508831.1:p.Gln553_Val557delinsHisAsnLeuProLeuTyr
ENST00000690917.1:n.1886_1897delinsCAACCTTCCACTGTA
ENST00000691361.1:n.578_589delinsCAACCTTCCACTGTA
ENST00000692783.1:c.1668_1679delinsCAACCTTCCACTGTA	ENSP00000508733.1:p.Gln556_Val560delinsHisAsnLeuProLeuTyr
ENST00000692991.1:n.1765_1776delinsCAACCTTCCACTGTA
ENST00000288135.6:c.1668_1679delinsCAACCTTCCACTGTA MANE Select	ENSP00000288135.6:p.Gln556_Val560delinsHisAsnLeuProLeuTyr
ENST00000288135.5:c.1668_1679delinsCAACCTTCCACTGTA	ENSP00000288135.5:p.Gln556_Val560delinsHisAsnLeuProLeuTyr
ENST00000412167.6:c.1656_1667delinsCAACCTTCCACTGTA	ENSP00000390987.2:p.Gln552_Val556delinsHisAsnLeuProLeuTyr
NM_000222.2:c.1668_1679delinsCAACCTTCCACTGTA , LRG_307t1:c.1668_1679delinsCAACCTTCCACTGTA	NP_000213.1:p.Gln556_Val560delinsHisAsnLeuProLeuTyr
NM_001093772.1:c.1656_1667delinsCAACCTTCCACTGTA	NP_001087241.1:p.Gln552_Val556delinsHisAsnLeuProLeuTyr
XM_005265740.1:c.1671_1682delinsCAACCTTCCACTGTA	XP_005265797.1:p.Gln557_Val561delinsHisAsnLeuProLeuTyr
XM_005265741.1:c.1671_1682delinsCAACCTTCCACTGTA	XP_005265798.1:p.Gln557_Val561delinsHisAsnLeuProLeuTyr
XM_005265742.1:c.1659_1670delinsCAACCTTCCACTGTA	XP_005265799.1:p.Gln553_Val557delinsHisAsnLeuProLeuTyr
XM_005265742.3:c.1659_1670delinsCAACCTTCCACTGTA	XP_005265799.1:p.Gln553_Val557delinsHisAsnLeuProLeuTyr
XM_017008178.1:c.1668_1679delinsCAACCTTCCACTGTA	XP_016863667.1:p.Gln556_Val560delinsHisAsnLeuProLeuTyr
XM_017008179.1:c.1659_1670delinsCAACCTTCCACTGTA	XP_016863668.1:p.Gln553_Val557delinsHisAsnLeuProLeuTyr
XM_017008180.1:c.1656_1667delinsCAACCTTCCACTGTA	XP_016863669.1:p.Gln552_Val556delinsHisAsnLeuProLeuTyr
NM_000222.3:c.1668_1679delinsCAACCTTCCACTGTA MANE Select	NP_000213.1:p.Gln556_Val560delinsHisAsnLeuProLeuTyr
NM_001093772.2:c.1656_1667delinsCAACCTTCCACTGTA	NP_001087241.1:p.Gln552_Val556delinsHisAsnLeuProLeuTyr
NM_001385284.1:c.1671_1682delinsCAACCTTCCACTGTA	NP_001372213.1:p.Gln557_Val561delinsHisAsnLeuProLeuTyr
NM_001385285.1:c.1668_1679delinsCAACCTTCCACTGTA	NP_001372214.1:p.Gln556_Val560delinsHisAsnLeuProLeuTyr
NM_001385286.1:c.1656_1667delinsCAACCTTCCACTGTA	NP_001372215.1:p.Gln552_Val556delinsHisAsnLeuProLeuTyr
NM_001385288.1:c.1659_1670delinsCAACCTTCCACTGTA	NP_001372217.1:p.Gln553_Val557delinsHisAsnLeuProLeuTyr
NM_001385290.1:c.1671_1682delinsCAACCTTCCACTGTA	NP_001372219.1:p.Gln557_Val561delinsHisAsnLeuProLeuTyr
NM_001385292.1:c.1659_1670delinsCAACCTTCCACTGTA	NP_001372221.1:p.Gln553_Val557delinsHisAsnLeuProLeuTyr