Canonical Allele Identifier: CA1458739173

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727649_54727650delinsGT , CM000666.2:g.54727649_54727650delinsGT	GRCh38
NC_000004.11:g.55593815_55593816delinsGT , CM000666.1:g.55593815_55593816delinsGT	GRCh37
NC_000004.10:g.55288572_55288573delinsGT	NCBI36
NG_007456.1:g.74655_74656delinsGT , LRG_307:g.74655_74656delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1765+107_1765+108delinsGT	ENSP00000390987.3:n.1765+107_1765+108delinsGT
ENST00000685269.1:n.1852+107_1852+108delinsGT
ENST00000686011.1:c.1762+107_1762+108delinsGT	ENSP00000509704.1:n.1762+107_1762+108delinsGT
ENST00000687109.1:c.1777+107_1777+108delinsGT	ENSP00000509371.1:n.1777+107_1777+108delinsGT
ENST00000687208.1:n.2189+107_2189+108delinsGT
ENST00000687246.1:c.1762+107_1762+108delinsGT	ENSP00000509114.1:n.1762+107_1762+108delinsGT
ENST00000687265.1:n.1932+107_1932+108delinsGT
ENST00000687295.1:c.1762+107_1762+108delinsGT	ENSP00000509450.1:n.1762+107_1762+108delinsGT
ENST00000689832.1:c.1777+107_1777+108delinsGT	ENSP00000509084.1:n.1777+107_1777+108delinsGT
ENST00000689994.1:c.1264+107_1264+108delinsGT	ENSP00000509156.1:n.1264+107_1264+108delinsGT
ENST00000690543.1:c.1765+107_1765+108delinsGT	ENSP00000508831.1:n.1765+107_1765+108delinsGT
ENST00000690917.1:n.1992+107_1992+108delinsGT
ENST00000691361.1:n.684+107_684+108delinsGT
ENST00000692783.1:c.1774+107_1774+108delinsGT	ENSP00000508733.1:n.1774+107_1774+108delinsGT
ENST00000692991.1:n.1871+107_1871+108delinsGT
ENST00000288135.6:c.1774+107_1774+108delinsGT MANE Select	ENSP00000288135.6:n.1774+107_1774+108delinsGT
ENST00000288135.5:c.1774+107_1774+108delinsGT	ENSP00000288135.5:n.1774+107_1774+108delinsGT
ENST00000412167.6:c.1762+107_1762+108delinsGT	ENSP00000390987.2:n.1762+107_1762+108delinsGT
NM_000222.2:c.1774+107_1774+108delinsGT , LRG_307t1:c.1774+107_1774+108delinsGT	NP_000213.1:n.1774+107_1774+108delinsGT
NM_001093772.1:c.1762+107_1762+108delinsGT	NP_001087241.1:n.1762+107_1762+108delinsGT
XM_005265740.1:c.1777+107_1777+108delinsGT	XP_005265797.1:n.1777+107_1777+108delinsGT
XM_005265741.1:c.1777+107_1777+108delinsGT	XP_005265798.1:n.1777+107_1777+108delinsGT
XM_005265742.1:c.1765+107_1765+108delinsGT	XP_005265799.1:n.1765+107_1765+108delinsGT
XM_005265742.3:c.1765+107_1765+108delinsGT	XP_005265799.1:n.1765+107_1765+108delinsGT
XM_017008178.1:c.1774+107_1774+108delinsGT	XP_016863667.1:n.1774+107_1774+108delinsGT
XM_017008179.1:c.1765+107_1765+108delinsGT	XP_016863668.1:n.1765+107_1765+108delinsGT
XM_017008180.1:c.1762+107_1762+108delinsGT	XP_016863669.1:n.1762+107_1762+108delinsGT
NM_000222.3:c.1774+107_1774+108delinsGT MANE Select	NP_000213.1:n.1774+107_1774+108delinsGT
NM_001093772.2:c.1762+107_1762+108delinsGT	NP_001087241.1:n.1762+107_1762+108delinsGT
NM_001385284.1:c.1777+107_1777+108delinsGT	NP_001372213.1:n.1777+107_1777+108delinsGT
NM_001385285.1:c.1774+107_1774+108delinsGT	NP_001372214.1:n.1774+107_1774+108delinsGT
NM_001385286.1:c.1762+107_1762+108delinsGT	NP_001372215.1:n.1762+107_1762+108delinsGT
NM_001385288.1:c.1765+107_1765+108delinsGT	NP_001372217.1:n.1765+107_1765+108delinsGT
NM_001385290.1:c.1777+107_1777+108delinsGT	NP_001372219.1:n.1777+107_1777+108delinsGT
NM_001385292.1:c.1765+107_1765+108delinsGT	NP_001372221.1:n.1765+107_1765+108delinsGT