Canonical Allele Identifier: CA1548129246
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859862A= , CM000667.2:g.56859862A= GRCh38
NC_000005.9:g.56155689A= , CM000667.1:g.56155689A= GRCh37
NC_000005.8:g.56191446A= NCBI36
NG_031884.1:g.49790A=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.781A= MANE Select ENSP00000382423.3:p.Thr261=
ENST00000399503.3:c.781A= ENSP00000382423.3:p.Thr261=
NM_005921.1:c.781A= NP_005912.1:p.Thr261=
XM_005248519.3:c.403A= XP_005248576.2:p.Thr135=
XM_011543406.1:c.526A= XP_011541708.1:p.Thr176=
XM_011543407.1:c.781A= XP_011541709.1:p.Thr261=
XM_011543408.1:c.781A= XP_011541710.1:p.Thr261=
XM_017009484.1:c.370A= XP_016864973.1:p.Thr124=
XM_017009485.1:c.292A= XP_016864974.1:p.Thr98=
XR_001742068.2:n.812A=
NM_005921.2:c.781A= MANE Select NP_005912.1:p.Thr261=