Canonical Allele Identifier: CA645516855
Gene: KIT HGNC NCBI

Linked Data

COSMIC: COSM96876

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54727442_54727494delinsCG , CM000666.2:g.54727442_54727494delinsCG GRCh38
NC_000004.11:g.55593608_55593660delinsCG , CM000666.1:g.55593608_55593660delinsCG GRCh37
NC_000004.10:g.55288365_55288417delinsCG NCBI36
NG_007456.1:g.74448_74500delinsCG , LRG_307:g.74448_74500delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.1665_1717delinsCG ENSP00000390987.3:p.Lys555_Leu573delinsAsnVal
ENST00000685269.1:n.1752_1804delinsCG
ENST00000686011.1:c.1662_1714delinsCG ENSP00000509704.1:p.Lys554_Leu572delinsAsnVal
ENST00000687109.1:c.1677_1729delinsCG ENSP00000509371.1:p.Lys559_Leu577delinsAsnVal
ENST00000687208.1:n.2089_2141delinsCG
ENST00000687246.1:c.1662_1714delinsCG ENSP00000509114.1:p.Lys554_Leu572delinsAsnVal
ENST00000687265.1:n.1832_1884delinsCG
ENST00000687295.1:c.1662_1714delinsCG ENSP00000509450.1:p.Lys554_Leu572delinsAsnVal
ENST00000689832.1:c.1677_1729delinsCG ENSP00000509084.1:p.Lys559_Leu577delinsAsnVal
ENST00000689994.1:c.1164_1216delinsCG ENSP00000509156.1:p.Lys388_Leu406delinsAsnVal
ENST00000690543.1:c.1665_1717delinsCG ENSP00000508831.1:p.Lys555_Leu573delinsAsnVal
ENST00000690917.1:n.1892_1944delinsCG
ENST00000691361.1:n.584_636delinsCG
ENST00000692783.1:c.1674_1726delinsCG ENSP00000508733.1:p.Lys558_Leu576delinsAsnVal
ENST00000692991.1:n.1771_1823delinsCG
ENST00000288135.6:c.1674_1726delinsCG MANE Select ENSP00000288135.6:p.Lys558_Leu576delinsAsnVal
ENST00000288135.5:c.1674_1726delinsCG ENSP00000288135.5:p.Lys558_Leu576delinsAsnVal
ENST00000412167.6:c.1662_1714delinsCG ENSP00000390987.2:p.Lys554_Leu572delinsAsnVal
NM_000222.2:c.1674_1726delinsCG , LRG_307t1:c.1674_1726delinsCG NP_000213.1:p.Lys558_Leu576delinsAsnVal
NM_001093772.1:c.1662_1714delinsCG NP_001087241.1:p.Lys554_Leu572delinsAsnVal
XM_005265740.1:c.1677_1729delinsCG XP_005265797.1:p.Lys559_Leu577delinsAsnVal
XM_005265741.1:c.1677_1729delinsCG XP_005265798.1:p.Lys559_Leu577delinsAsnVal
XM_005265742.1:c.1665_1717delinsCG XP_005265799.1:p.Lys555_Leu573delinsAsnVal
XM_005265742.3:c.1665_1717delinsCG XP_005265799.1:p.Lys555_Leu573delinsAsnVal
XM_017008178.1:c.1674_1726delinsCG XP_016863667.1:p.Lys558_Leu576delinsAsnVal
XM_017008179.1:c.1665_1717delinsCG XP_016863668.1:p.Lys555_Leu573delinsAsnVal
XM_017008180.1:c.1662_1714delinsCG XP_016863669.1:p.Lys554_Leu572delinsAsnVal
NM_000222.3:c.1674_1726delinsCG MANE Select NP_000213.1:p.Lys558_Leu576delinsAsnVal
NM_001093772.2:c.1662_1714delinsCG NP_001087241.1:p.Lys554_Leu572delinsAsnVal
NM_001385284.1:c.1677_1729delinsCG NP_001372213.1:p.Lys559_Leu577delinsAsnVal
NM_001385285.1:c.1674_1726delinsCG NP_001372214.1:p.Lys558_Leu576delinsAsnVal
NM_001385286.1:c.1662_1714delinsCG NP_001372215.1:p.Lys554_Leu572delinsAsnVal
NM_001385288.1:c.1665_1717delinsCG NP_001372217.1:p.Lys555_Leu573delinsAsnVal
NM_001385290.1:c.1677_1729delinsCG NP_001372219.1:p.Lys559_Leu577delinsAsnVal
NM_001385292.1:c.1665_1717delinsCG NP_001372221.1:p.Lys555_Leu573delinsAsnVal