Canonical Allele Identifier: CA1548129193
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859752A= , CM000667.2:g.56859752A= GRCh38
NC_000005.9:g.56155579A= , CM000667.1:g.56155579A= GRCh37
NC_000005.8:g.56191336A= NCBI36
NG_031884.1:g.49680A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.671A= MANE Select ENSP00000382423.3:p.Glu224=
ENST00000399503.3:c.671A= ENSP00000382423.3:p.Glu224=
NM_005921.1:c.671A= NP_005912.1:p.Glu224=
XM_005248519.3:c.293A= XP_005248576.2:p.Glu98=
XM_011543406.1:c.416A= XP_011541708.1:p.Glu139=
XM_011543407.1:c.671A= XP_011541709.1:p.Glu224=
XM_011543408.1:c.671A= XP_011541710.1:p.Glu224=
XM_017009484.1:c.260A= XP_016864973.1:p.Glu87=
XM_017009485.1:c.182A= XP_016864974.1:p.Glu61=
XR_001742068.2:n.702A=
NM_005921.2:c.671A= MANE Select NP_005912.1:p.Glu224=