Canonical Allele Identifier: CA444399220

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111942445
• MyVariant Identifiers: chr5:g.56177721G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881894G>A , CM000667.2:g.56881894G>A	GRCh38
NC_000005.9:g.56177721G>A , CM000667.1:g.56177721G>A	GRCh37
NC_000005.8:g.56213478G>A	NCBI36
NG_031884.1:g.71822G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2694G>A MANE Select	ENSP00000382423.3:p.Glu898=
ENST00000399503.3:c.2694G>A	ENSP00000382423.3:p.Glu898=
NM_005921.1:c.2694G>A	NP_005912.1:p.Glu898=
XM_005248519.3:c.2316G>A	XP_005248576.2:p.Glu772=
XM_011543406.1:c.2439G>A	XP_011541708.1:p.Glu813=
XM_011543407.1:c.2415G>A	XP_011541709.1:p.Glu805=
XM_011543408.1:c.2694G>A	XP_011541710.1:p.Glu898=
XM_017009484.1:c.2283G>A	XP_016864973.1:p.Glu761=
XM_017009485.1:c.2205G>A	XP_016864974.1:p.Glu735=
XR_001742068.2:n.2725G>A
NM_005921.2:c.2694G>A MANE Select	NP_005912.1:p.Glu898=