Canonical Allele Identifier: CA1548129216
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859804T= , CM000667.2:g.56859804T= GRCh38
NC_000005.9:g.56155631T= , CM000667.1:g.56155631T= GRCh37
NC_000005.8:g.56191388T= NCBI36
NG_031884.1:g.49732T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.723T= MANE Select ENSP00000382423.3:p.Ala241=
ENST00000399503.3:c.723T= ENSP00000382423.3:p.Ala241=
NM_005921.1:c.723T= NP_005912.1:p.Ala241=
XM_005248519.3:c.345T= XP_005248576.2:p.Ala115=
XM_011543406.1:c.468T= XP_011541708.1:p.Ala156=
XM_011543407.1:c.723T= XP_011541709.1:p.Ala241=
XM_011543408.1:c.723T= XP_011541710.1:p.Ala241=
XM_017009484.1:c.312T= XP_016864973.1:p.Ala104=
XM_017009485.1:c.234T= XP_016864974.1:p.Ala78=
XR_001742068.2:n.754T=
NM_005921.2:c.723T= MANE Select NP_005912.1:p.Ala241=