Canonical Allele Identifier: CA645516730
Gene: KIT HGNC NCBI

Linked Data

COSMIC: COSM6142

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54727413_54727440del , CM000666.2:g.54727413_54727440del GRCh38
NC_000004.11:g.55593579_55593606del , CM000666.1:g.55593579_55593606del GRCh37
NC_000004.10:g.55288336_55288363del NCBI36
NG_007456.1:g.74419_74446del , LRG_307:g.74419_74446del

Transcript Alleles

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