Canonical Allele Identifier: CA359787819

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1244452250
• MyVariant Identifiers: chr5:g.56178200A>G (hg19) ; chr5:g.56882373A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882373A>G , CM000667.2:g.56882373A>G	GRCh38
NC_000005.9:g.56178200A>G , CM000667.1:g.56178200A>G	GRCh37
NC_000005.8:g.56213957A>G	NCBI36
NG_031884.1:g.72301A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3173A>G MANE Select	ENSP00000382423.3:p.His1058Arg
ENST00000399503.3:c.3173A>G	ENSP00000382423.3:p.His1058Arg
NM_005921.1:c.3173A>G	NP_005912.1:p.His1058Arg
XM_005248519.3:c.2795A>G	XP_005248576.2:p.His932Arg
XM_011543406.1:c.2918A>G	XP_011541708.1:p.His973Arg
XM_011543407.1:c.2894A>G	XP_011541709.1:p.His965Arg
XM_011543408.1:c.3173A>G	XP_011541710.1:p.His1058Arg
XM_017009484.1:c.2762A>G	XP_016864973.1:p.His921Arg
XM_017009485.1:c.2684A>G	XP_016864974.1:p.His895Arg
XR_001742068.2:n.3204A>G
NM_005921.2:c.3173A>G MANE Select	NP_005912.1:p.His1058Arg