Canonical Allele Identifier: CA359780679

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1747982445
• MyVariant Identifiers: chr5:g.56170931C>A (hg19) ; chr5:g.56875104C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875104C>A , CM000667.2:g.56875104C>A	GRCh38
NC_000005.9:g.56170931C>A , CM000667.1:g.56170931C>A	GRCh37
NC_000005.8:g.56206688C>A	NCBI36
NG_031884.1:g.65032C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1759C>A MANE Select	ENSP00000382423.3:p.Leu587Ile
ENST00000399503.3:c.1759C>A	ENSP00000382423.3:p.Leu587Ile
NM_005921.1:c.1759C>A	NP_005912.1:p.Leu587Ile
XM_005248519.3:c.1381C>A	XP_005248576.2:p.Leu461Ile
XM_011543406.1:c.1504C>A	XP_011541708.1:p.Leu502Ile
XM_011543407.1:c.1686+2099C>A	XP_011541709.1:n.1686+2099C>A
XM_011543408.1:c.1759C>A	XP_011541710.1:p.Leu587Ile
XM_017009484.1:c.1348C>A	XP_016864973.1:p.Leu450Ile
XM_017009485.1:c.1270C>A	XP_016864974.1:p.Leu424Ile
XR_001742068.2:n.1790C>A
NM_005921.2:c.1759C>A MANE Select	NP_005912.1:p.Leu587Ile