Canonical Allele Identifier: CA359781034

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111921243
• MyVariant Identifiers: chr5:g.56171025C>G (hg19) ; chr5:g.56875198C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875198C>G , CM000667.2:g.56875198C>G	GRCh38
NC_000005.9:g.56171025C>G , CM000667.1:g.56171025C>G	GRCh37
NC_000005.8:g.56206782C>G	NCBI36
NG_031884.1:g.65126C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1853C>G MANE Select	ENSP00000382423.3:p.Ala618Gly
ENST00000399503.3:c.1853C>G	ENSP00000382423.3:p.Ala618Gly
NM_005921.1:c.1853C>G	NP_005912.1:p.Ala618Gly
XM_005248519.3:c.1475C>G	XP_005248576.2:p.Ala492Gly
XM_011543406.1:c.1598C>G	XP_011541708.1:p.Ala533Gly
XM_011543407.1:c.1686+2193C>G	XP_011541709.1:n.1686+2193C>G
XM_011543408.1:c.1853C>G	XP_011541710.1:p.Ala618Gly
XM_017009484.1:c.1442C>G	XP_016864973.1:p.Ala481Gly
XM_017009485.1:c.1364C>G	XP_016864974.1:p.Ala455Gly
XR_001742068.2:n.1884C>G
NM_005921.2:c.1853C>G MANE Select	NP_005912.1:p.Ala618Gly