Canonical Allele Identifier: CA359787625

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111945511
• MyVariant Identifiers: chr5:g.56178115C>A (hg19) ; chr5:g.56882288C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882288C>A , CM000667.2:g.56882288C>A	GRCh38
NC_000005.9:g.56178115C>A , CM000667.1:g.56178115C>A	GRCh37
NC_000005.8:g.56213872C>A	NCBI36
NG_031884.1:g.72216C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3088C>A MANE Select	ENSP00000382423.3:p.His1030Asn
ENST00000399503.3:c.3088C>A	ENSP00000382423.3:p.His1030Asn
NM_005921.1:c.3088C>A	NP_005912.1:p.His1030Asn
XM_005248519.3:c.2710C>A	XP_005248576.2:p.His904Asn
XM_011543406.1:c.2833C>A	XP_011541708.1:p.His945Asn
XM_011543407.1:c.2809C>A	XP_011541709.1:p.His937Asn
XM_011543408.1:c.3088C>A	XP_011541710.1:p.His1030Asn
XM_017009484.1:c.2677C>A	XP_016864973.1:p.His893Asn
XM_017009485.1:c.2599C>A	XP_016864974.1:p.His867Asn
XR_001742068.2:n.3119C>A
NM_005921.2:c.3088C>A MANE Select	NP_005912.1:p.His1030Asn