Canonical Allele Identifier: CA2145333327
Gene: MAP3K9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.70727459G= , CM000676.2:g.70727459G= GRCh38
NC_000014.8:g.71194176G= , CM000676.1:g.71194176G= GRCh37
NC_000014.7:g.70263929G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000554752.7:c.*2921C= MANE Select ENSP00000451612.2:n.*2921C=
ENST00000554752.6:c.6236C= ENSP00000451612.2:n.6236C=
ENST00000611979.4:c.5564C= ENSP00000480011.1:n.5564C=
NM_001284230.1:c.6236C= NP_001271159.1:n.6236C=
NM_001284231.1:c.*2921C= NP_001271160.1:n.*2921C=
NM_001284232.1:c.*2921C= NP_001271161.1:n.*2921C=
NM_033141.3:c.6278C= NP_149132.2:n.6278C=
XM_005267683.3:c.*2921C= XP_005267740.1:n.*2921C=
XM_011536788.1:c.*2921C= XP_011535090.1:n.*2921C=
XM_011536789.1:c.*2921C= XP_011535091.1:n.*2921C=
XM_011536790.1:c.*2921C= XP_011535092.1:n.*2921C=
XM_011536791.1:c.*2921C= XP_011535093.1:n.*2921C=
XM_011536792.1:c.*2921C= XP_011535094.1:n.*2921C=
XM_011536793.1:c.*2921C= XP_011535095.1:n.*2921C=
XM_011536794.1:c.*2921C= XP_011535096.1:n.*2921C=
XM_005267683.5:c.*2921C= XP_005267740.1:n.*2921C=
XM_011536788.3:c.*2921C= XP_011535090.1:n.*2921C=
XM_011536794.2:c.*2921C= XP_011535096.1:n.*2921C=
NM_033141.4:c.*2921C= NP_149132.2:n.*2921C=
NM_001284230.2:c.*2921C= MANE Select NP_001271159.1:n.*2921C=