Canonical Allele Identifier: CA359802427

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1747447963
• MyVariant Identifiers: chr5:g.56155594C>T (hg19) ; chr5:g.56859767C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859767C>T , CM000667.2:g.56859767C>T	GRCh38
NC_000005.9:g.56155594C>T , CM000667.1:g.56155594C>T	GRCh37
NC_000005.8:g.56191351C>T	NCBI36
NG_031884.1:g.49695C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.686C>T MANE Select	ENSP00000382423.3:p.Ala229Val
ENST00000399503.3:c.686C>T	ENSP00000382423.3:p.Ala229Val
NM_005921.1:c.686C>T	NP_005912.1:p.Ala229Val
XM_005248519.3:c.308C>T	XP_005248576.2:p.Ala103Val
XM_011543406.1:c.431C>T	XP_011541708.1:p.Ala144Val
XM_011543407.1:c.686C>T	XP_011541709.1:p.Ala229Val
XM_011543408.1:c.686C>T	XP_011541710.1:p.Ala229Val
XM_017009484.1:c.275C>T	XP_016864973.1:p.Ala92Val
XM_017009485.1:c.197C>T	XP_016864974.1:p.Ala66Val
XR_001742068.2:n.717C>T
NM_005921.2:c.686C>T MANE Select	NP_005912.1:p.Ala229Val