Canonical Allele Identifier: CA1548129203
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859781G= , CM000667.2:g.56859781G= GRCh38
NC_000005.9:g.56155608G= , CM000667.1:g.56155608G= GRCh37
NC_000005.8:g.56191365G= NCBI36
NG_031884.1:g.49709G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.700G= MANE Select ENSP00000382423.3:p.Gly234=
ENST00000399503.3:c.700G= ENSP00000382423.3:p.Gly234=
NM_005921.1:c.700G= NP_005912.1:p.Gly234=
XM_005248519.3:c.322G= XP_005248576.2:p.Gly108=
XM_011543406.1:c.445G= XP_011541708.1:p.Gly149=
XM_011543407.1:c.700G= XP_011541709.1:p.Gly234=
XM_011543408.1:c.700G= XP_011541710.1:p.Gly234=
XM_017009484.1:c.289G= XP_016864973.1:p.Gly97=
XM_017009485.1:c.211G= XP_016864974.1:p.Gly71=
XR_001742068.2:n.731G=
NM_005921.2:c.700G= MANE Select NP_005912.1:p.Gly234=