Canonical Allele Identifier: CA2142951670
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076620G= , CM000676.2:g.65076620G= GRCh38
NC_000014.8:g.65543338G= , CM000676.1:g.65543338G= GRCh37
NC_000014.7:g.64613091G= NCBI36
NG_029830.1:g.30890C= , LRG_530:g.30890C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.120C= ENSP00000452206.2:p.Thr40=
ENST00000556979.6:c.*792C= ENSP00000452378.1:n.*792C=
ENST00000358664.9:c.339C= MANE Select ENSP00000351490.4:p.Thr113=
ENST00000651648.1:c.145-6251C= ENSP00000498863.1:n.145-6251C=
ENST00000284165.10:c.*1183C= ENSP00000284165.6:n.*1183C=
ENST00000341653.6:c.171+17088C= ENSP00000342482.2:n.171+17088C=
ENST00000358402.8:c.312C= ENSP00000351175.4:p.Thr104=
ENST00000358664.8:c.339C= ENSP00000351490.4:p.Thr113=
ENST00000394606.6:c.*112C= ENSP00000378104.2:n.*112C=
ENST00000553928.5:c.*128C= ENSP00000451907.1:n.*128C=
ENST00000555419.5:c.231C= ENSP00000452405.1:p.Thr77=
ENST00000555932.5:c.80C= ENSP00000450763.1:p.Pro27=
ENST00000556892.5:c.120C= ENSP00000452206.1:p.Thr40=
ENST00000557277.5:c.150C= ENSP00000450955.1:p.Thr50=
ENST00000618858.4:c.*128C= ENSP00000480127.1:n.*128C=
NM_001271069.1:c.144+17088C= NP_001257998.1:n.144+17088C=
NM_002382.4:c.339C= NP_002373.3:p.Thr113=
NM_145112.2:c.312C= NP_660087.1:p.Thr104=
NM_145113.2:c.*128C= NP_660088.1:n.*128C=
NM_197957.3:c.171+17088C= NP_932061.1:n.171+17088C=
NR_073137.1:n.463C=
XR_429315.2:n.626C=
XR_943450.1:n.707C=
XR_943451.1:n.723C=
XR_943452.1:n.669C=
NM_001320415.1:c.150C= NP_001307344.1:p.Thr50=
XM_017021312.2:c.150C= XP_016876801.1:p.Thr50=
XM_017021313.1:c.150C= XP_016876802.1:p.Thr50=
XR_001750326.2:n.684C=
XR_001750327.2:n.603C=
XR_002957553.1:n.1117C=
XR_943450.3:n.707C=
XR_943451.3:n.723C=
XR_943452.3:n.668C=
NM_001320415.2:c.150C= NP_001307344.1:p.Thr50=
NM_002382.5:c.339C= MANE Select NP_002373.3:p.Thr113=
NM_145112.3:c.312C= NP_660087.1:p.Thr104=
NM_145113.3:c.*128C= NP_660088.1:n.*128C=
NM_001271069.2:c.144+17088C= NP_001257998.1:n.144+17088C=
NM_197957.4:c.171+17088C= NP_932061.1:n.171+17088C=