Canonical Allele Identifier: CA359802367

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155569G>A (hg19) ; chr5:g.56859742G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859742G>A , CM000667.2:g.56859742G>A	GRCh38
NC_000005.9:g.56155569G>A , CM000667.1:g.56155569G>A	GRCh37
NC_000005.8:g.56191326G>A	NCBI36
NG_031884.1:g.49670G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.661G>A MANE Select	ENSP00000382423.3:p.Asp221Asn
ENST00000399503.3:c.661G>A	ENSP00000382423.3:p.Asp221Asn
NM_005921.1:c.661G>A	NP_005912.1:p.Asp221Asn
XM_005248519.3:c.283G>A	XP_005248576.2:p.Asp95Asn
XM_011543406.1:c.406G>A	XP_011541708.1:p.Asp136Asn
XM_011543407.1:c.661G>A	XP_011541709.1:p.Asp221Asn
XM_011543408.1:c.661G>A	XP_011541710.1:p.Asp221Asn
XM_017009484.1:c.250G>A	XP_016864973.1:p.Asp84Asn
XM_017009485.1:c.172G>A	XP_016864974.1:p.Asp58Asn
XR_001742068.2:n.692G>A
NM_005921.2:c.661G>A MANE Select	NP_005912.1:p.Asp221Asn