Canonical Allele Identifier: CA359785766

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177450C>A (hg19) ; chr5:g.56881623C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881623C>A , CM000667.2:g.56881623C>A	GRCh38
NC_000005.9:g.56177450C>A , CM000667.1:g.56177450C>A	GRCh37
NC_000005.8:g.56213207C>A	NCBI36
NG_031884.1:g.71551C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2423C>A MANE Select	ENSP00000382423.3:p.Ser808Tyr
ENST00000399503.3:c.2423C>A	ENSP00000382423.3:p.Ser808Tyr
NM_005921.1:c.2423C>A	NP_005912.1:p.Ser808Tyr
XM_005248519.3:c.2045C>A	XP_005248576.2:p.Ser682Tyr
XM_011543406.1:c.2168C>A	XP_011541708.1:p.Ser723Tyr
XM_011543407.1:c.2144C>A	XP_011541709.1:p.Ser715Tyr
XM_011543408.1:c.2423C>A	XP_011541710.1:p.Ser808Tyr
XM_017009484.1:c.2012C>A	XP_016864973.1:p.Ser671Tyr
XM_017009485.1:c.1934C>A	XP_016864974.1:p.Ser645Tyr
XR_001742068.2:n.2454C>A
NM_005921.2:c.2423C>A MANE Select	NP_005912.1:p.Ser808Tyr