Canonical Allele Identifier: CA359786212

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177659G>A (hg19) ; chr5:g.56881832G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881832G>A , CM000667.2:g.56881832G>A	GRCh38
NC_000005.9:g.56177659G>A , CM000667.1:g.56177659G>A	GRCh37
NC_000005.8:g.56213416G>A	NCBI36
NG_031884.1:g.71760G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2632G>A MANE Select	ENSP00000382423.3:p.Asp878Asn
ENST00000399503.3:c.2632G>A	ENSP00000382423.3:p.Asp878Asn
NM_005921.1:c.2632G>A	NP_005912.1:p.Asp878Asn
XM_005248519.3:c.2254G>A	XP_005248576.2:p.Asp752Asn
XM_011543406.1:c.2377G>A	XP_011541708.1:p.Asp793Asn
XM_011543407.1:c.2353G>A	XP_011541709.1:p.Asp785Asn
XM_011543408.1:c.2632G>A	XP_011541710.1:p.Asp878Asn
XM_017009484.1:c.2221G>A	XP_016864973.1:p.Asp741Asn
XM_017009485.1:c.2143G>A	XP_016864974.1:p.Asp715Asn
XR_001742068.2:n.2663G>A
NM_005921.2:c.2632G>A MANE Select	NP_005912.1:p.Asp878Asn