Canonical Allele Identifier: CA645516726
Gene: KIT HGNC NCBI

Linked Data

COSMIC: COSM19322

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54727407_54727440del , CM000666.2:g.54727407_54727440del GRCh38
NC_000004.11:g.55593573_55593606del , CM000666.1:g.55593573_55593606del GRCh37
NC_000004.10:g.55288330_55288363del NCBI36
NG_007456.1:g.74413_74446del , LRG_307:g.74413_74446del

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.1639-9_1663del
ENST00000685269.1:n.1726-9_1750del
ENST00000686011.1:c.1636-9_1660del
ENST00000687109.1:c.1651-9_1675del
ENST00000687208.1:n.2063-9_2087del
ENST00000687246.1:c.1636-9_1660del
ENST00000687265.1:n.1806-9_1830del
ENST00000687295.1:c.1636-9_1660del
ENST00000689832.1:c.1651-9_1675del
ENST00000689994.1:c.1138-9_1162del
ENST00000690543.1:c.1639-9_1663del
ENST00000690917.1:n.1866-9_1890del
ENST00000691361.1:n.558-9_582del
ENST00000692783.1:c.1648-9_1672del
ENST00000692991.1:n.1745-9_1769del
ENST00000288135.6:c.1648-9_1672del
ENST00000288135.5:c.1648-9_1672del
ENST00000412167.6:c.1636-9_1660del
NM_000222.2:c.1648-9_1672del , LRG_307t1:c.1648-9_1672del
NM_001093772.1:c.1636-9_1660del
XM_005265740.1:c.1651-9_1675del
XM_005265741.1:c.1651-9_1675del
XM_005265742.1:c.1639-9_1663del
XM_005265742.3:c.1639-9_1663del
XM_017008178.1:c.1648-9_1672del
XM_017008179.1:c.1639-9_1663del
XM_017008180.1:c.1636-9_1660del
NM_000222.3:c.1648-9_1672del
NM_001093772.2:c.1636-9_1660del
NM_001385284.1:c.1651-9_1675del
NM_001385285.1:c.1648-9_1672del
NM_001385286.1:c.1636-9_1660del
NM_001385288.1:c.1639-9_1663del
NM_001385290.1:c.1651-9_1675del
NM_001385292.1:c.1639-9_1663del