Canonical Allele Identifier: CA359802386
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859751G>A , CM000667.2:g.56859751G>A GRCh38
NC_000005.9:g.56155578G>A , CM000667.1:g.56155578G>A GRCh37
NC_000005.8:g.56191335G>A NCBI36
NG_031884.1:g.49679G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.670G>A MANE Select ENSP00000382423.3:p.Glu224Lys
ENST00000399503.3:c.670G>A ENSP00000382423.3:p.Glu224Lys
NM_005921.1:c.670G>A NP_005912.1:p.Glu224Lys
XM_005248519.3:c.292G>A XP_005248576.2:p.Glu98Lys
XM_011543406.1:c.415G>A XP_011541708.1:p.Glu139Lys
XM_011543407.1:c.670G>A XP_011541709.1:p.Glu224Lys
XM_011543408.1:c.670G>A XP_011541710.1:p.Glu224Lys
XM_017009484.1:c.259G>A XP_016864973.1:p.Glu87Lys
XM_017009485.1:c.181G>A XP_016864974.1:p.Glu61Lys
XR_001742068.2:n.701G>A
NM_005921.2:c.670G>A MANE Select NP_005912.1:p.Glu224Lys