Canonical Allele Identifier: CA645516732

Gene: KIT

Linked Data

• COSMIC: COSM5622359

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727416_54727438del , CM000666.2:g.54727416_54727438del	GRCh38
NC_000004.11:g.55593582_55593604del , CM000666.1:g.55593582_55593604del	GRCh37
NC_000004.10:g.55288339_55288361del	NCBI36
NG_007456.1:g.74422_74444del , LRG_307:g.74422_74444del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1639_1661del
ENST00000685269.1:n.1726_1748del
ENST00000686011.1:c.1636_1658del
ENST00000687109.1:c.1651_1673del
ENST00000687208.1:n.2063_2085del
ENST00000687246.1:c.1636_1658del
ENST00000687265.1:n.1806_1828del
ENST00000687295.1:c.1636_1658del
ENST00000689832.1:c.1651_1673del
ENST00000689994.1:c.1138_1160del
ENST00000690543.1:c.1639_1661del
ENST00000690917.1:n.1866_1888del
ENST00000691361.1:n.558_580del
ENST00000692783.1:c.1648_1670del
ENST00000692991.1:n.1745_1767del
ENST00000288135.6:c.1648_1670del
ENST00000288135.5:c.1648_1670del
ENST00000412167.6:c.1636_1658del
NM_000222.2:c.1648_1670del , LRG_307t1:c.1648_1670del
NM_001093772.1:c.1636_1658del
XM_005265740.1:c.1651_1673del
XM_005265741.1:c.1651_1673del
XM_005265742.1:c.1639_1661del
XM_005265742.3:c.1639_1661del
XM_017008178.1:c.1648_1670del
XM_017008179.1:c.1639_1661del
XM_017008180.1:c.1636_1658del
NM_000222.3:c.1648_1670del
NM_001093772.2:c.1636_1658del
NM_001385284.1:c.1651_1673del
NM_001385285.1:c.1648_1670del
NM_001385286.1:c.1636_1658del
NM_001385288.1:c.1639_1661del
NM_001385290.1:c.1651_1673del
NM_001385292.1:c.1639_1661del