Canonical Allele Identifier: CA359785765

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177449T>G (hg19) ; chr5:g.56881622T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881622T>G , CM000667.2:g.56881622T>G	GRCh38
NC_000005.9:g.56177449T>G , CM000667.1:g.56177449T>G	GRCh37
NC_000005.8:g.56213206T>G	NCBI36
NG_031884.1:g.71550T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2422T>G MANE Select	ENSP00000382423.3:p.Ser808Ala
ENST00000399503.3:c.2422T>G	ENSP00000382423.3:p.Ser808Ala
NM_005921.1:c.2422T>G	NP_005912.1:p.Ser808Ala
XM_005248519.3:c.2044T>G	XP_005248576.2:p.Ser682Ala
XM_011543406.1:c.2167T>G	XP_011541708.1:p.Ser723Ala
XM_011543407.1:c.2143T>G	XP_011541709.1:p.Ser715Ala
XM_011543408.1:c.2422T>G	XP_011541710.1:p.Ser808Ala
XM_017009484.1:c.2011T>G	XP_016864973.1:p.Ser671Ala
XM_017009485.1:c.1933T>G	XP_016864974.1:p.Ser645Ala
XR_001742068.2:n.2453T>G
NM_005921.2:c.2422T>G MANE Select	NP_005912.1:p.Ser808Ala