Canonical Allele Identifier: CA1548129204
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859785A= , CM000667.2:g.56859785A= GRCh38
NC_000005.9:g.56155612A= , CM000667.1:g.56155612A= GRCh37
NC_000005.8:g.56191369A= NCBI36
NG_031884.1:g.49713A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.704A= MANE Select ENSP00000382423.3:p.Glu235=
ENST00000399503.3:c.704A= ENSP00000382423.3:p.Glu235=
NM_005921.1:c.704A= NP_005912.1:p.Glu235=
XM_005248519.3:c.326A= XP_005248576.2:p.Glu109=
XM_011543406.1:c.449A= XP_011541708.1:p.Glu150=
XM_011543407.1:c.704A= XP_011541709.1:p.Glu235=
XM_011543408.1:c.704A= XP_011541710.1:p.Glu235=
XM_017009484.1:c.293A= XP_016864973.1:p.Glu98=
XM_017009485.1:c.215A= XP_016864974.1:p.Glu72=
XR_001742068.2:n.735A=
NM_005921.2:c.704A= MANE Select NP_005912.1:p.Glu235=