Canonical Allele Identifier: CA359787422

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111944536
• MyVariant Identifiers: chr5:g.56178019G>A (hg19) ; chr5:g.56882192G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882192G>A , CM000667.2:g.56882192G>A	GRCh38
NC_000005.9:g.56178019G>A , CM000667.1:g.56178019G>A	GRCh37
NC_000005.8:g.56213776G>A	NCBI36
NG_031884.1:g.72120G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2992G>A MANE Select	ENSP00000382423.3:p.Ala998Thr
ENST00000399503.3:c.2992G>A	ENSP00000382423.3:p.Ala998Thr
NM_005921.1:c.2992G>A	NP_005912.1:p.Ala998Thr
XM_005248519.3:c.2614G>A	XP_005248576.2:p.Ala872Thr
XM_011543406.1:c.2737G>A	XP_011541708.1:p.Ala913Thr
XM_011543407.1:c.2713G>A	XP_011541709.1:p.Ala905Thr
XM_011543408.1:c.2992G>A	XP_011541710.1:p.Ala998Thr
XM_017009484.1:c.2581G>A	XP_016864973.1:p.Ala861Thr
XM_017009485.1:c.2503G>A	XP_016864974.1:p.Ala835Thr
XR_001742068.2:n.3023G>A
NM_005921.2:c.2992G>A MANE Select	NP_005912.1:p.Ala998Thr