Canonical Allele Identifier: CA359780675

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56170928C>G (hg19) ; chr5:g.56875101C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875101C>G , CM000667.2:g.56875101C>G	GRCh38
NC_000005.9:g.56170928C>G , CM000667.1:g.56170928C>G	GRCh37
NC_000005.8:g.56206685C>G	NCBI36
NG_031884.1:g.65029C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1756C>G MANE Select	ENSP00000382423.3:p.Arg586Gly
ENST00000399503.3:c.1756C>G	ENSP00000382423.3:p.Arg586Gly
NM_005921.1:c.1756C>G	NP_005912.1:p.Arg586Gly
XM_005248519.3:c.1378C>G	XP_005248576.2:p.Arg460Gly
XM_011543406.1:c.1501C>G	XP_011541708.1:p.Arg501Gly
XM_011543407.1:c.1686+2096C>G	XP_011541709.1:n.1686+2096C>G
XM_011543408.1:c.1756C>G	XP_011541710.1:p.Arg586Gly
XM_017009484.1:c.1345C>G	XP_016864973.1:p.Arg449Gly
XM_017009485.1:c.1267C>G	XP_016864974.1:p.Arg423Gly
XR_001742068.2:n.1787C>G
NM_005921.2:c.1756C>G MANE Select	NP_005912.1:p.Arg586Gly