Canonical Allele Identifier: CA2142951639
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076556C= , CM000676.2:g.65076556C= GRCh38
NC_000014.8:g.65543274C= , CM000676.1:g.65543274C= GRCh37
NC_000014.7:g.64613027C= NCBI36
NG_029830.1:g.30954G= , LRG_530:g.30954G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.184G= ENSP00000452206.2:p.Asp62=
ENST00000556979.6:c.*856G= ENSP00000452378.1:n.*856G=
ENST00000358664.9:c.403G= MANE Select ENSP00000351490.4:p.Asp135=
ENST00000651648.1:c.145-6187G= ENSP00000498863.1:n.145-6187G=
ENST00000284165.10:c.*1247G= ENSP00000284165.6:n.*1247G=
ENST00000341653.6:c.171+17152G= ENSP00000342482.2:n.171+17152G=
ENST00000358402.8:c.376G= ENSP00000351175.4:p.Asp126=
ENST00000358664.8:c.403G= ENSP00000351490.4:p.Asp135=
ENST00000394606.6:c.*176G= ENSP00000378104.2:n.*176G=
ENST00000553928.5:c.*192G= ENSP00000451907.1:n.*192G=
ENST00000555419.5:c.295G= ENSP00000452405.1:p.Asp99=
ENST00000555932.5:c.144G= ENSP00000450763.1:p.Ser48=
ENST00000557277.5:c.214G= ENSP00000450955.1:p.Asp72=
ENST00000618858.4:c.*192G= ENSP00000480127.1:n.*192G=
NM_001271069.1:c.144+17152G= NP_001257998.1:n.144+17152G=
NM_002382.4:c.403G= NP_002373.3:p.Asp135=
NM_145112.2:c.376G= NP_660087.1:p.Asp126=
NM_145113.2:c.*192G= NP_660088.1:n.*192G=
NM_197957.3:c.171+17152G= NP_932061.1:n.171+17152G=
NR_073137.1:n.527G=
XR_429315.2:n.690G=
NM_001320415.1:c.214G= NP_001307344.1:p.Asp72=
XM_017021312.2:c.214G= XP_016876801.1:p.Asp72=
XM_017021313.1:c.214G= XP_016876802.1:p.Asp72=
XR_001750326.2:n.748G=
XR_001750327.2:n.667G=
XR_002957553.1:n.1181G=
XR_943450.3:n.771G=
XR_943451.3:n.787G=
XR_943452.3:n.732G=
NM_001320415.2:c.214G= NP_001307344.1:p.Asp72=
NM_002382.5:c.403G= MANE Select NP_002373.3:p.Asp135=
NM_145112.3:c.376G= NP_660087.1:p.Asp126=
NM_145113.3:c.*192G= NP_660088.1:n.*192G=
NM_001271069.2:c.144+17152G= NP_001257998.1:n.144+17152G=
NM_197957.4:c.171+17152G= NP_932061.1:n.171+17152G=