Canonical Allele Identifier: CA891841833

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727406_54727440del , CM000666.2:g.54727406_54727440del	GRCh38
NC_000004.11:g.55593572_55593606del , CM000666.1:g.55593572_55593606del	GRCh37
NC_000004.10:g.55288329_55288363del	NCBI36
NG_007456.1:g.74412_74446del , LRG_307:g.74412_74446del

Transcript Alleles

HGVS	Amino-acid change
ENST00000412167.7:c.1639-10_1663del
ENST00000685269.1:n.1726-10_1750del
ENST00000686011.1:c.1636-10_1660del
ENST00000687109.1:c.1651-10_1675del
ENST00000687208.1:n.2063-10_2087del
ENST00000687246.1:c.1636-10_1660del
ENST00000687265.1:n.1806-10_1830del
ENST00000687295.1:c.1636-10_1660del
ENST00000689832.1:c.1651-10_1675del
ENST00000689994.1:c.1138-10_1162del
ENST00000690543.1:c.1639-10_1663del
ENST00000690917.1:n.1866-10_1890del
ENST00000691361.1:n.558-10_582del
ENST00000692783.1:c.1648-10_1672del
ENST00000692991.1:n.1745-10_1769del
ENST00000288135.6:c.1648-10_1672del
ENST00000288135.5:c.1648-10_1672del
ENST00000412167.6:c.1636-10_1660del
NM_000222.2:c.1648-10_1672del , LRG_307t1:c.1648-10_1672del
NM_001093772.1:c.1636-10_1660del
XM_005265740.1:c.1651-10_1675del
XM_005265741.1:c.1651-10_1675del
XM_005265742.1:c.1639-10_1663del
XM_005265742.3:c.1639-10_1663del
XM_017008178.1:c.1648-10_1672del
XM_017008179.1:c.1639-10_1663del
XM_017008180.1:c.1636-10_1660del
NM_000222.3:c.1648-10_1672del
NM_001093772.2:c.1636-10_1660del
NM_001385284.1:c.1651-10_1675del
NM_001385285.1:c.1648-10_1672del
NM_001385286.1:c.1636-10_1660del
NM_001385288.1:c.1639-10_1663del
NM_001385290.1:c.1651-10_1675del
NM_001385292.1:c.1639-10_1663del