Canonical Allele Identifier: CA359802515

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111874184
• MyVariant Identifiers: chr5:g.56155639C>A (hg19) ; chr5:g.56859812C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859812C>A , CM000667.2:g.56859812C>A	GRCh38
NC_000005.9:g.56155639C>A , CM000667.1:g.56155639C>A	GRCh37
NC_000005.8:g.56191396C>A	NCBI36
NG_031884.1:g.49740C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.731C>A MANE Select	ENSP00000382423.3:p.Ala244Asp
ENST00000399503.3:c.731C>A	ENSP00000382423.3:p.Ala244Asp
NM_005921.1:c.731C>A	NP_005912.1:p.Ala244Asp
XM_005248519.3:c.353C>A	XP_005248576.2:p.Ala118Asp
XM_011543406.1:c.476C>A	XP_011541708.1:p.Ala159Asp
XM_011543407.1:c.731C>A	XP_011541709.1:p.Ala244Asp
XM_011543408.1:c.731C>A	XP_011541710.1:p.Ala244Asp
XM_017009484.1:c.320C>A	XP_016864973.1:p.Ala107Asp
XM_017009485.1:c.242C>A	XP_016864974.1:p.Ala81Asp
XR_001742068.2:n.762C>A
NM_005921.2:c.731C>A MANE Select	NP_005912.1:p.Ala244Asp