Canonical Allele Identifier: CA444399145

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1332290542
• MyVariant Identifiers: chr5:g.56177565C>G (hg19) ; chr5:g.56881738C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881738C>G , CM000667.2:g.56881738C>G	GRCh38
NC_000005.9:g.56177565C>G , CM000667.1:g.56177565C>G	GRCh37
NC_000005.8:g.56213322C>G	NCBI36
NG_031884.1:g.71666C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2538C>G MANE Select	ENSP00000382423.3:p.Ser846=
ENST00000399503.3:c.2538C>G	ENSP00000382423.3:p.Ser846=
NM_005921.1:c.2538C>G	NP_005912.1:p.Ser846=
XM_005248519.3:c.2160C>G	XP_005248576.2:p.Ser720=
XM_011543406.1:c.2283C>G	XP_011541708.1:p.Ser761=
XM_011543407.1:c.2259C>G	XP_011541709.1:p.Ser753=
XM_011543408.1:c.2538C>G	XP_011541710.1:p.Ser846=
XM_017009484.1:c.2127C>G	XP_016864973.1:p.Ser709=
XM_017009485.1:c.2049C>G	XP_016864974.1:p.Ser683=
XR_001742068.2:n.2569C>G
NM_005921.2:c.2538C>G MANE Select	NP_005912.1:p.Ser846=