Canonical Allele Identifier: CA359786429

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177724C>A (hg19) ; chr5:g.56881897C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881897C>A , CM000667.2:g.56881897C>A	GRCh38
NC_000005.9:g.56177724C>A , CM000667.1:g.56177724C>A	GRCh37
NC_000005.8:g.56213481C>A	NCBI36
NG_031884.1:g.71825C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2697C>A MANE Select	ENSP00000382423.3:p.Asn899Lys
ENST00000399503.3:c.2697C>A	ENSP00000382423.3:p.Asn899Lys
NM_005921.1:c.2697C>A	NP_005912.1:p.Asn899Lys
XM_005248519.3:c.2319C>A	XP_005248576.2:p.Asn773Lys
XM_011543406.1:c.2442C>A	XP_011541708.1:p.Asn814Lys
XM_011543407.1:c.2418C>A	XP_011541709.1:p.Asn806Lys
XM_011543408.1:c.2697C>A	XP_011541710.1:p.Asn899Lys
XM_017009484.1:c.2286C>A	XP_016864973.1:p.Asn762Lys
XM_017009485.1:c.2208C>A	XP_016864974.1:p.Asn736Lys
XR_001742068.2:n.2728C>A
NM_005921.2:c.2697C>A MANE Select	NP_005912.1:p.Asn899Lys