Canonical Allele Identifier: CA1458747072
Gene: KIT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54736501C= , CM000666.2:g.54736501C= GRCh38
NC_000004.11:g.55602667C= , CM000666.1:g.55602667C= GRCh37
NC_000004.10:g.55297424C= NCBI36
NG_007456.1:g.83507C= , LRG_307:g.83507C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.2476C= ENSP00000390987.3:p.Arg826=
ENST00000684818.1:n.1180C=
ENST00000685269.1:n.2566C=
ENST00000686011.1:c.2473C= ENSP00000509704.1:p.Arg825=
ENST00000687109.1:c.2491C= ENSP00000509371.1:p.Arg831=
ENST00000687208.1:n.2900C=
ENST00000687246.1:c.2353C= ENSP00000509114.1:p.Arg785=
ENST00000687265.1:n.2646C=
ENST00000687295.1:c.2476C= ENSP00000509450.1:p.Arg826=
ENST00000688060.1:n.285C=
ENST00000689832.1:c.2488C= ENSP00000509084.1:p.Arg830=
ENST00000689994.1:c.1978C= ENSP00000509156.1:p.Arg660=
ENST00000690543.1:c.2479C= ENSP00000508831.1:p.Arg827=
ENST00000690917.1:n.2706C=
ENST00000691361.1:n.1398C=
ENST00000692301.1:n.1180C=
ENST00000692783.1:c.2485C= ENSP00000508733.1:p.Arg829=
ENST00000692991.1:n.2585C=
ENST00000288135.6:c.2488C= MANE Select ENSP00000288135.6:p.Arg830=
ENST00000288135.5:c.2488C= ENSP00000288135.5:p.Arg830=
ENST00000412167.6:c.2476C= ENSP00000390987.2:p.Arg826=
NM_000222.2:c.2488C= , LRG_307t1:c.2488C= NP_000213.1:p.Arg830=
NM_001093772.1:c.2476C= NP_001087241.1:p.Arg826=
XM_005265740.1:c.2491C= XP_005265797.1:p.Arg831=
XM_005265741.1:c.2488C= XP_005265798.1:p.Arg830=
XM_005265742.1:c.2479C= XP_005265799.1:p.Arg827=
XM_005265742.3:c.2479C= XP_005265799.1:p.Arg827=
XM_017008178.1:c.2485C= XP_016863667.1:p.Arg829=
XM_017008179.1:c.2476C= XP_016863668.1:p.Arg826=
XM_017008180.1:c.2473C= XP_016863669.1:p.Arg825=
NM_000222.3:c.2488C= MANE Select NP_000213.1:p.Arg830=
NM_001093772.2:c.2476C= NP_001087241.1:p.Arg826=
NM_001385284.1:c.2491C= NP_001372213.1:p.Arg831=
NM_001385285.1:c.2485C= NP_001372214.1:p.Arg829=
NM_001385286.1:c.2473C= NP_001372215.1:p.Arg825=
NM_001385288.1:c.2479C= NP_001372217.1:p.Arg827=
NM_001385290.1:c.2488C= NP_001372219.1:p.Arg830=
NM_001385292.1:c.2476C= NP_001372221.1:p.Arg826=