Canonical Allele Identifier: CA1458739164

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727643_54727644delinsCA , CM000666.2:g.54727643_54727644delinsCA	GRCh38
NC_000004.11:g.55593809_55593810delinsCA , CM000666.1:g.55593809_55593810delinsCA	GRCh37
NC_000004.10:g.55288566_55288567delinsCA	NCBI36
NG_007456.1:g.74649_74650delinsCA , LRG_307:g.74649_74650delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1765+101_1765+102delinsCA	ENSP00000390987.3:n.1765+101_1765+102delinsCA
ENST00000685269.1:n.1852+101_1852+102delinsCA
ENST00000686011.1:c.1762+101_1762+102delinsCA	ENSP00000509704.1:n.1762+101_1762+102delinsCA
ENST00000687109.1:c.1777+101_1777+102delinsCA	ENSP00000509371.1:n.1777+101_1777+102delinsCA
ENST00000687208.1:n.2189+101_2189+102delinsCA
ENST00000687246.1:c.1762+101_1762+102delinsCA	ENSP00000509114.1:n.1762+101_1762+102delinsCA
ENST00000687265.1:n.1932+101_1932+102delinsCA
ENST00000687295.1:c.1762+101_1762+102delinsCA	ENSP00000509450.1:n.1762+101_1762+102delinsCA
ENST00000689832.1:c.1777+101_1777+102delinsCA	ENSP00000509084.1:n.1777+101_1777+102delinsCA
ENST00000689994.1:c.1264+101_1264+102delinsCA	ENSP00000509156.1:n.1264+101_1264+102delinsCA
ENST00000690543.1:c.1765+101_1765+102delinsCA	ENSP00000508831.1:n.1765+101_1765+102delinsCA
ENST00000690917.1:n.1992+101_1992+102delinsCA
ENST00000691361.1:n.684+101_684+102delinsCA
ENST00000692783.1:c.1774+101_1774+102delinsCA	ENSP00000508733.1:n.1774+101_1774+102delinsCA
ENST00000692991.1:n.1871+101_1871+102delinsCA
ENST00000288135.6:c.1774+101_1774+102delinsCA MANE Select	ENSP00000288135.6:n.1774+101_1774+102delinsCA
ENST00000288135.5:c.1774+101_1774+102delinsCA	ENSP00000288135.5:n.1774+101_1774+102delinsCA
ENST00000412167.6:c.1762+101_1762+102delinsCA	ENSP00000390987.2:n.1762+101_1762+102delinsCA
NM_000222.2:c.1774+101_1774+102delinsCA , LRG_307t1:c.1774+101_1774+102delinsCA	NP_000213.1:n.1774+101_1774+102delinsCA
NM_001093772.1:c.1762+101_1762+102delinsCA	NP_001087241.1:n.1762+101_1762+102delinsCA
XM_005265740.1:c.1777+101_1777+102delinsCA	XP_005265797.1:n.1777+101_1777+102delinsCA
XM_005265741.1:c.1777+101_1777+102delinsCA	XP_005265798.1:n.1777+101_1777+102delinsCA
XM_005265742.1:c.1765+101_1765+102delinsCA	XP_005265799.1:n.1765+101_1765+102delinsCA
XM_005265742.3:c.1765+101_1765+102delinsCA	XP_005265799.1:n.1765+101_1765+102delinsCA
XM_017008178.1:c.1774+101_1774+102delinsCA	XP_016863667.1:n.1774+101_1774+102delinsCA
XM_017008179.1:c.1765+101_1765+102delinsCA	XP_016863668.1:n.1765+101_1765+102delinsCA
XM_017008180.1:c.1762+101_1762+102delinsCA	XP_016863669.1:n.1762+101_1762+102delinsCA
NM_000222.3:c.1774+101_1774+102delinsCA MANE Select	NP_000213.1:n.1774+101_1774+102delinsCA
NM_001093772.2:c.1762+101_1762+102delinsCA	NP_001087241.1:n.1762+101_1762+102delinsCA
NM_001385284.1:c.1777+101_1777+102delinsCA	NP_001372213.1:n.1777+101_1777+102delinsCA
NM_001385285.1:c.1774+101_1774+102delinsCA	NP_001372214.1:n.1774+101_1774+102delinsCA
NM_001385286.1:c.1762+101_1762+102delinsCA	NP_001372215.1:n.1762+101_1762+102delinsCA
NM_001385288.1:c.1765+101_1765+102delinsCA	NP_001372217.1:n.1765+101_1765+102delinsCA
NM_001385290.1:c.1777+101_1777+102delinsCA	NP_001372219.1:n.1777+101_1777+102delinsCA
NM_001385292.1:c.1765+101_1765+102delinsCA	NP_001372221.1:n.1765+101_1765+102delinsCA