Canonical Allele Identifier: CA356913448
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1469646
ClinVar RCV Id: RCV001973071
dbSNP Id: rs2109811701

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54736604C>G , CM000666.2:g.54736604C>G GRCh38
NC_000004.11:g.55602770C>G , CM000666.1:g.55602770C>G GRCh37
NC_000004.10:g.55297527C>G NCBI36
NG_007456.1:g.83610C>G , LRG_307:g.83610C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.2579C>G ENSP00000390987.3:p.Ser860Cys
ENST00000684818.1:n.1283C>G
ENST00000685269.1:n.2669C>G
ENST00000686011.1:c.2576C>G ENSP00000509704.1:p.Ser859Cys
ENST00000687109.1:c.2594C>G ENSP00000509371.1:p.Ser865Cys
ENST00000687208.1:n.3003C>G
ENST00000687246.1:c.2456C>G ENSP00000509114.1:p.Ser819Cys
ENST00000687265.1:n.2749C>G
ENST00000687295.1:c.2579C>G ENSP00000509450.1:p.Ser860Cys
ENST00000688060.1:n.388C>G
ENST00000689832.1:c.2591C>G ENSP00000509084.1:p.Ser864Cys
ENST00000689994.1:c.2081C>G ENSP00000509156.1:p.Ser694Cys
ENST00000690543.1:c.2582C>G ENSP00000508831.1:p.Ser861Cys
ENST00000690917.1:n.2809C>G
ENST00000691361.1:n.1501C>G
ENST00000692301.1:n.1283C>G
ENST00000692783.1:c.2588C>G ENSP00000508733.1:p.Ser863Cys
ENST00000692991.1:n.2688C>G
ENST00000288135.6:c.2591C>G MANE Select ENSP00000288135.6:p.Ser864Cys
ENST00000288135.5:c.2591C>G ENSP00000288135.5:p.Ser864Cys
ENST00000412167.6:c.2579C>G ENSP00000390987.2:p.Ser860Cys
NM_000222.2:c.2591C>G , LRG_307t1:c.2591C>G NP_000213.1:p.Ser864Cys
NM_001093772.1:c.2579C>G NP_001087241.1:p.Ser860Cys
XM_005265740.1:c.2594C>G XP_005265797.1:p.Ser865Cys
XM_005265741.1:c.2591C>G XP_005265798.1:p.Ser864Cys
XM_005265742.1:c.2582C>G XP_005265799.1:p.Ser861Cys
XM_005265742.3:c.2582C>G XP_005265799.1:p.Ser861Cys
XM_017008178.1:c.2588C>G XP_016863667.1:p.Ser863Cys
XM_017008179.1:c.2579C>G XP_016863668.1:p.Ser860Cys
XM_017008180.1:c.2576C>G XP_016863669.1:p.Ser859Cys
NM_000222.3:c.2591C>G MANE Select NP_000213.1:p.Ser864Cys
NM_001093772.2:c.2579C>G NP_001087241.1:p.Ser860Cys
NM_001385284.1:c.2594C>G NP_001372213.1:p.Ser865Cys
NM_001385285.1:c.2588C>G NP_001372214.1:p.Ser863Cys
NM_001385286.1:c.2576C>G NP_001372215.1:p.Ser859Cys
NM_001385288.1:c.2582C>G NP_001372217.1:p.Ser861Cys
NM_001385290.1:c.2591C>G NP_001372219.1:p.Ser864Cys
NM_001385292.1:c.2579C>G NP_001372221.1:p.Ser860Cys