Canonical Allele Identifier: CA359786099

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177606C>G (hg19) ; chr5:g.56881779C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881779C>G , CM000667.2:g.56881779C>G	GRCh38
NC_000005.9:g.56177606C>G , CM000667.1:g.56177606C>G	GRCh37
NC_000005.8:g.56213363C>G	NCBI36
NG_031884.1:g.71707C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2579C>G MANE Select	ENSP00000382423.3:p.Ala860Gly
ENST00000399503.3:c.2579C>G	ENSP00000382423.3:p.Ala860Gly
NM_005921.1:c.2579C>G	NP_005912.1:p.Ala860Gly
XM_005248519.3:c.2201C>G	XP_005248576.2:p.Ala734Gly
XM_011543406.1:c.2324C>G	XP_011541708.1:p.Ala775Gly
XM_011543407.1:c.2300C>G	XP_011541709.1:p.Ala767Gly
XM_011543408.1:c.2579C>G	XP_011541710.1:p.Ala860Gly
XM_017009484.1:c.2168C>G	XP_016864973.1:p.Ala723Gly
XM_017009485.1:c.2090C>G	XP_016864974.1:p.Ala697Gly
XR_001742068.2:n.2610C>G
NM_005921.2:c.2579C>G MANE Select	NP_005912.1:p.Ala860Gly