Canonical Allele Identifier: CA1548129192
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.670G= MANE Select ENSP00000382423.3:p.Glu224=
ENST00000399503.3:c.670G= ENSP00000382423.3:p.Glu224=
NM_005921.1:c.670G= NP_005912.1:p.Glu224=
XM_005248519.3:c.292G= XP_005248576.2:p.Glu98=
XM_011543406.1:c.415G= XP_011541708.1:p.Glu139=
XM_011543407.1:c.670G= XP_011541709.1:p.Glu224=
XM_011543408.1:c.670G= XP_011541710.1:p.Glu224=
XM_017009484.1:c.259G= XP_016864973.1:p.Glu87=
XM_017009485.1:c.181G= XP_016864974.1:p.Glu61=
XR_001742068.2:n.701G=
NM_005921.2:c.670G= MANE Select NP_005912.1:p.Glu224=