Canonical Allele Identifier: CA359787482

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111944815
• MyVariant Identifiers: chr5:g.56178047A>G (hg19) ; chr5:g.56882220A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882220A>G , CM000667.2:g.56882220A>G	GRCh38
NC_000005.9:g.56178047A>G , CM000667.1:g.56178047A>G	GRCh37
NC_000005.8:g.56213804A>G	NCBI36
NG_031884.1:g.72148A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3020A>G MANE Select	ENSP00000382423.3:p.Gln1007Arg
ENST00000399503.3:c.3020A>G	ENSP00000382423.3:p.Gln1007Arg
NM_005921.1:c.3020A>G	NP_005912.1:p.Gln1007Arg
XM_005248519.3:c.2642A>G	XP_005248576.2:p.Gln881Arg
XM_011543406.1:c.2765A>G	XP_011541708.1:p.Gln922Arg
XM_011543407.1:c.2741A>G	XP_011541709.1:p.Gln914Arg
XM_011543408.1:c.3020A>G	XP_011541710.1:p.Gln1007Arg
XM_017009484.1:c.2609A>G	XP_016864973.1:p.Gln870Arg
XM_017009485.1:c.2531A>G	XP_016864974.1:p.Gln844Arg
XR_001742068.2:n.3051A>G
NM_005921.2:c.3020A>G MANE Select	NP_005912.1:p.Gln1007Arg