Canonical Allele Identifier: CA1458739659
Gene: KIT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54728031C= , CM000666.2:g.54728031C= GRCh38
NC_000004.11:g.55594197C= , CM000666.1:g.55594197C= GRCh37
NC_000004.10:g.55288954C= NCBI36
NG_007456.1:g.75037C= , LRG_307:g.75037C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.1891C= ENSP00000390987.3:p.Arg631=
ENST00000685269.1:n.1978C=
ENST00000686011.1:c.1888C= ENSP00000509704.1:p.Arg630=
ENST00000687109.1:c.1903C= ENSP00000509371.1:p.Arg635=
ENST00000687208.1:n.2315C=
ENST00000687246.1:c.1888C= ENSP00000509114.1:p.Arg630=
ENST00000687265.1:n.2058C=
ENST00000687295.1:c.1888C= ENSP00000509450.1:p.Arg630=
ENST00000689832.1:c.1903C= ENSP00000509084.1:p.Arg635=
ENST00000689994.1:c.1390C= ENSP00000509156.1:p.Arg464=
ENST00000690543.1:c.1891C= ENSP00000508831.1:p.Arg631=
ENST00000690917.1:n.2118C=
ENST00000691361.1:n.810C=
ENST00000692783.1:c.1900C= ENSP00000508733.1:p.Arg634=
ENST00000692991.1:n.1997C=
ENST00000288135.6:c.1900C= MANE Select ENSP00000288135.6:p.Arg634=
ENST00000288135.5:c.1900C= ENSP00000288135.5:p.Arg634=
ENST00000412167.6:c.1888C= ENSP00000390987.2:p.Arg630=
NM_000222.2:c.1900C= , LRG_307t1:c.1900C= NP_000213.1:p.Arg634=
NM_001093772.1:c.1888C= NP_001087241.1:p.Arg630=
XM_005265740.1:c.1903C= XP_005265797.1:p.Arg635=
XM_005265741.1:c.1903C= XP_005265798.1:p.Arg635=
XM_005265742.1:c.1891C= XP_005265799.1:p.Arg631=
XM_005265742.3:c.1891C= XP_005265799.1:p.Arg631=
XM_017008178.1:c.1900C= XP_016863667.1:p.Arg634=
XM_017008179.1:c.1891C= XP_016863668.1:p.Arg631=
XM_017008180.1:c.1888C= XP_016863669.1:p.Arg630=
NM_000222.3:c.1900C= MANE Select NP_000213.1:p.Arg634=
NM_001093772.2:c.1888C= NP_001087241.1:p.Arg630=
NM_001385284.1:c.1903C= NP_001372213.1:p.Arg635=
NM_001385285.1:c.1900C= NP_001372214.1:p.Arg634=
NM_001385286.1:c.1888C= NP_001372215.1:p.Arg630=
NM_001385288.1:c.1891C= NP_001372217.1:p.Arg631=
NM_001385290.1:c.1903C= NP_001372219.1:p.Arg635=
NM_001385292.1:c.1891C= NP_001372221.1:p.Arg631=