Canonical Allele Identifier: CA2142951373
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075992G= , CM000676.2:g.65075992G= GRCh38
NC_000014.8:g.65542710G= , CM000676.1:g.65542710G= GRCh37
NC_000014.7:g.64612463G= NCBI36
NG_029830.1:g.31518C= , LRG_530:g.31518C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*484C= ENSP00000452206.2:n.*484C=
ENST00000556979.6:c.*1420C= ENSP00000452378.1:n.*1420C=
ENST00000358664.9:c.*484C= MANE Select ENSP00000351490.4:n.*484C=
ENST00000651648.1:c.145-5623C= ENSP00000498863.1:n.145-5623C=
ENST00000284165.10:c.*1811C= ENSP00000284165.6:n.*1811C=
ENST00000341653.6:c.171+17716C= ENSP00000342482.2:n.171+17716C=
ENST00000358402.8:c.*484C= ENSP00000351175.4:n.*484C=
ENST00000358664.8:c.*484C= ENSP00000351490.4:n.*484C=
ENST00000394606.6:c.*740C= ENSP00000378104.2:n.*740C=
ENST00000555932.5:c.*459C= ENSP00000450763.1:n.*459C=
ENST00000618858.4:c.*756C= ENSP00000480127.1:n.*756C=
NM_001271069.1:c.144+17716C= NP_001257998.1:n.144+17716C=
NM_002382.4:c.*484C= NP_002373.3:n.*484C=
NM_145112.2:c.*484C= NP_660087.1:n.*484C=
NM_145113.2:c.*756C= NP_660088.1:n.*756C=
NM_197957.3:c.171+17716C= NP_932061.1:n.171+17716C=
NR_073137.1:n.1091C=
XR_429315.2:n.1254C=
NM_001320415.1:c.*484C= NP_001307344.1:n.*484C=
XM_017021312.2:c.*484C= XP_016876801.1:n.*484C=
XM_017021313.1:c.*484C= XP_016876802.1:n.*484C=
XR_001750326.2:n.1312C=
XR_001750327.2:n.1231C=
XR_002957553.1:n.1745C=
XR_943450.3:n.1335C=
XR_943451.3:n.1351C=
XR_943452.3:n.1296C=
NM_001320415.2:c.*484C= NP_001307344.1:n.*484C=
NM_002382.5:c.*484C= MANE Select NP_002373.3:n.*484C=
NM_145112.3:c.*484C= NP_660087.1:n.*484C=
NM_145113.3:c.*756C= NP_660088.1:n.*756C=
NM_001271069.2:c.144+17716C= NP_001257998.1:n.144+17716C=
NM_197957.4:c.171+17716C= NP_932061.1:n.171+17716C=