Canonical Allele Identifier: CA356913035
Gene: KIT HGNC NCBI

Linked Data

dbSNP Id: rs2109811101

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54736529A>T , CM000666.2:g.54736529A>T GRCh38
NC_000004.11:g.55602695A>T , CM000666.1:g.55602695A>T GRCh37
NC_000004.10:g.55297452A>T NCBI36
NG_007456.1:g.83535A>T , LRG_307:g.83535A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000412167.7:c.2504A>T ENSP00000390987.3:p.Glu835Val
ENST00000684818.1:n.1208A>T
ENST00000685269.1:n.2594A>T
ENST00000686011.1:c.2501A>T ENSP00000509704.1:p.Glu834Val
ENST00000687109.1:c.2519A>T ENSP00000509371.1:p.Glu840Val
ENST00000687208.1:n.2928A>T
ENST00000687246.1:c.2381A>T ENSP00000509114.1:p.Glu794Val
ENST00000687265.1:n.2674A>T
ENST00000687295.1:c.2504A>T ENSP00000509450.1:p.Glu835Val
ENST00000688060.1:n.313A>T
ENST00000689832.1:c.2516A>T ENSP00000509084.1:p.Glu839Val
ENST00000689994.1:c.2006A>T ENSP00000509156.1:p.Glu669Val
ENST00000690543.1:c.2507A>T ENSP00000508831.1:p.Glu836Val
ENST00000690917.1:n.2734A>T
ENST00000691361.1:n.1426A>T
ENST00000692301.1:n.1208A>T
ENST00000692783.1:c.2513A>T ENSP00000508733.1:p.Glu838Val
ENST00000692991.1:n.2613A>T
ENST00000288135.6:c.2516A>T MANE Select ENSP00000288135.6:p.Glu839Val
ENST00000288135.5:c.2516A>T ENSP00000288135.5:p.Glu839Val
ENST00000412167.6:c.2504A>T ENSP00000390987.2:p.Glu835Val
NM_000222.2:c.2516A>T , LRG_307t1:c.2516A>T NP_000213.1:p.Glu839Val
NM_001093772.1:c.2504A>T NP_001087241.1:p.Glu835Val
XM_005265740.1:c.2519A>T XP_005265797.1:p.Glu840Val
XM_005265741.1:c.2516A>T XP_005265798.1:p.Glu839Val
XM_005265742.1:c.2507A>T XP_005265799.1:p.Glu836Val
XM_005265742.3:c.2507A>T XP_005265799.1:p.Glu836Val
XM_017008178.1:c.2513A>T XP_016863667.1:p.Glu838Val
XM_017008179.1:c.2504A>T XP_016863668.1:p.Glu835Val
XM_017008180.1:c.2501A>T XP_016863669.1:p.Glu834Val
NM_000222.3:c.2516A>T MANE Select NP_000213.1:p.Glu839Val
NM_001093772.2:c.2504A>T NP_001087241.1:p.Glu835Val
NM_001385284.1:c.2519A>T NP_001372213.1:p.Glu840Val
NM_001385285.1:c.2513A>T NP_001372214.1:p.Glu838Val
NM_001385286.1:c.2501A>T NP_001372215.1:p.Glu834Val
NM_001385288.1:c.2507A>T NP_001372217.1:p.Glu836Val
NM_001385290.1:c.2516A>T NP_001372219.1:p.Glu839Val
NM_001385292.1:c.2504A>T NP_001372221.1:p.Glu835Val