Canonical Allele Identifier: CA359802655

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1335465628
• MyVariant Identifiers: chr5:g.56155711G>A (hg19) ; chr5:g.56859884G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859884G>A , CM000667.2:g.56859884G>A	GRCh38
NC_000005.9:g.56155711G>A , CM000667.1:g.56155711G>A	GRCh37
NC_000005.8:g.56191468G>A	NCBI36
NG_031884.1:g.49812G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.803G>A MANE Select	ENSP00000382423.3:p.Gly268Glu
ENST00000399503.3:c.803G>A	ENSP00000382423.3:p.Gly268Glu
NM_005921.1:c.803G>A	NP_005912.1:p.Gly268Glu
XM_005248519.3:c.425G>A	XP_005248576.2:p.Gly142Glu
XM_011543406.1:c.548G>A	XP_011541708.1:p.Gly183Glu
XM_011543407.1:c.803G>A	XP_011541709.1:p.Gly268Glu
XM_011543408.1:c.803G>A	XP_011541710.1:p.Gly268Glu
XM_017009484.1:c.392G>A	XP_016864973.1:p.Gly131Glu
XM_017009485.1:c.314G>A	XP_016864974.1:p.Gly105Glu
XR_001742068.2:n.834G>A
NM_005921.2:c.803G>A MANE Select	NP_005912.1:p.Gly268Glu