Canonical Allele Identifier: CA359786086

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1748215916
• MyVariant Identifiers: chr5:g.56177600C>G (hg19) ; chr5:g.56881773C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881773C>G , CM000667.2:g.56881773C>G	GRCh38
NC_000005.9:g.56177600C>G , CM000667.1:g.56177600C>G	GRCh37
NC_000005.8:g.56213357C>G	NCBI36
NG_031884.1:g.71701C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2573C>G MANE Select	ENSP00000382423.3:p.Ala858Gly
ENST00000399503.3:c.2573C>G	ENSP00000382423.3:p.Ala858Gly
NM_005921.1:c.2573C>G	NP_005912.1:p.Ala858Gly
XM_005248519.3:c.2195C>G	XP_005248576.2:p.Ala732Gly
XM_011543406.1:c.2318C>G	XP_011541708.1:p.Ala773Gly
XM_011543407.1:c.2294C>G	XP_011541709.1:p.Ala765Gly
XM_011543408.1:c.2573C>G	XP_011541710.1:p.Ala858Gly
XM_017009484.1:c.2162C>G	XP_016864973.1:p.Ala721Gly
XM_017009485.1:c.2084C>G	XP_016864974.1:p.Ala695Gly
XR_001742068.2:n.2604C>G
NM_005921.2:c.2573C>G MANE Select	NP_005912.1:p.Ala858Gly