Canonical Allele Identifier: CA645516898
Gene: KIT HGNC NCBI

Linked Data

COSMIC: COSM23417

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54727479_54727505dup , CM000666.2:g.54727479_54727505dup GRCh38
NC_000004.11:g.55593645_55593671dup , CM000666.1:g.55593645_55593671dup GRCh37
NC_000004.10:g.55288402_55288428dup NCBI36
NG_007456.1:g.74485_74511dup , LRG_307:g.74485_74511dup

Transcript Alleles

HGVS Amino-acid change
ENST00000412167.7:c.1702_1728dup ENSP00000390987.3:p.Asp576_His577insIleAspProThrGlnLeuProTyrA...
ENST00000685269.1:n.1789_1815dup
ENST00000686011.1:c.1699_1725dup ENSP00000509704.1:p.Asp575_His576insIleAspProThrGlnLeuProTyrA...
ENST00000687109.1:c.1714_1740dup ENSP00000509371.1:p.Asp580_His581insIleAspProThrGlnLeuProTyrA...
ENST00000687208.1:n.2126_2152dup
ENST00000687246.1:c.1699_1725dup ENSP00000509114.1:p.Asp575_His576insIleAspProThrGlnLeuProTyrA...
ENST00000687265.1:n.1869_1895dup
ENST00000687295.1:c.1699_1725dup ENSP00000509450.1:p.Asp575_His576insIleAspProThrGlnLeuProTyrA...
ENST00000689832.1:c.1714_1740dup ENSP00000509084.1:p.Asp580_His581insIleAspProThrGlnLeuProTyrA...
ENST00000689994.1:c.1201_1227dup ENSP00000509156.1:p.Asp409_His410insIleAspProThrGlnLeuProTyrA...
ENST00000690543.1:c.1702_1728dup ENSP00000508831.1:p.Asp576_His577insIleAspProThrGlnLeuProTyrA...
ENST00000690917.1:n.1929_1955dup
ENST00000691361.1:n.621_647dup
ENST00000692783.1:c.1711_1737dup ENSP00000508733.1:p.Asp579_His580insIleAspProThrGlnLeuProTyrA...
ENST00000692991.1:n.1808_1834dup
ENST00000288135.6:c.1711_1737dup MANE Select ENSP00000288135.6:p.Asp579_His580insIleAspProThrGlnLeuProTyrA...
ENST00000288135.5:c.1711_1737dup ENSP00000288135.5:p.Asp579_His580insIleAspProThrGlnLeuProTyrA...
ENST00000412167.6:c.1699_1725dup ENSP00000390987.2:p.Asp575_His576insIleAspProThrGlnLeuProTyrA...
NM_000222.2:c.1711_1737dup , LRG_307t1:c.1711_1737dup NP_000213.1:p.Asp579_His580insIleAspProThrGlnLeuProTyrAsp
NM_001093772.1:c.1699_1725dup NP_001087241.1:p.Asp575_His576insIleAspProThrGlnLeuProTyrAsp
XM_005265740.1:c.1714_1740dup XP_005265797.1:p.Asp580_His581insIleAspProThrGlnLeuProTyrAsp
XM_005265741.1:c.1714_1740dup XP_005265798.1:p.Asp580_His581insIleAspProThrGlnLeuProTyrAsp
XM_005265742.1:c.1702_1728dup XP_005265799.1:p.Asp576_His577insIleAspProThrGlnLeuProTyrAsp
XM_005265742.3:c.1702_1728dup XP_005265799.1:p.Asp576_His577insIleAspProThrGlnLeuProTyrAsp
XM_017008178.1:c.1711_1737dup XP_016863667.1:p.Asp579_His580insIleAspProThrGlnLeuProTyrAsp
XM_017008179.1:c.1702_1728dup XP_016863668.1:p.Asp576_His577insIleAspProThrGlnLeuProTyrAsp
XM_017008180.1:c.1699_1725dup XP_016863669.1:p.Asp575_His576insIleAspProThrGlnLeuProTyrAsp
NM_000222.3:c.1711_1737dup MANE Select NP_000213.1:p.Asp579_His580insIleAspProThrGlnLeuProTyrAsp
NM_001093772.2:c.1699_1725dup NP_001087241.1:p.Asp575_His576insIleAspProThrGlnLeuProTyrAsp
NM_001385284.1:c.1714_1740dup NP_001372213.1:p.Asp580_His581insIleAspProThrGlnLeuProTyrAsp
NM_001385285.1:c.1711_1737dup NP_001372214.1:p.Asp579_His580insIleAspProThrGlnLeuProTyrAsp
NM_001385286.1:c.1699_1725dup NP_001372215.1:p.Asp575_His576insIleAspProThrGlnLeuProTyrAsp
NM_001385288.1:c.1702_1728dup NP_001372217.1:p.Asp576_His577insIleAspProThrGlnLeuProTyrAsp
NM_001385290.1:c.1714_1740dup NP_001372219.1:p.Asp580_His581insIleAspProThrGlnLeuProTyrAsp
NM_001385292.1:c.1702_1728dup NP_001372221.1:p.Asp576_His577insIleAspProThrGlnLeuProTyrAsp