Canonical Allele Identifier: CA444399227

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1456715307
• MyVariant Identifiers: chr5:g.56177643C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881816C>A , CM000667.2:g.56881816C>A	GRCh38
NC_000005.9:g.56177643C>A , CM000667.1:g.56177643C>A	GRCh37
NC_000005.8:g.56213400C>A	NCBI36
NG_031884.1:g.71744C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2616C>A MANE Select	ENSP00000382423.3:p.Gly872=
ENST00000399503.3:c.2616C>A	ENSP00000382423.3:p.Gly872=
NM_005921.1:c.2616C>A	NP_005912.1:p.Gly872=
XM_005248519.3:c.2238C>A	XP_005248576.2:p.Gly746=
XM_011543406.1:c.2361C>A	XP_011541708.1:p.Gly787=
XM_011543407.1:c.2337C>A	XP_011541709.1:p.Gly779=
XM_011543408.1:c.2616C>A	XP_011541710.1:p.Gly872=
XM_017009484.1:c.2205C>A	XP_016864973.1:p.Gly735=
XM_017009485.1:c.2127C>A	XP_016864974.1:p.Gly709=
XR_001742068.2:n.2647C>A
NM_005921.2:c.2616C>A MANE Select	NP_005912.1:p.Gly872=