Canonical Allele Identifier: CA2142951196
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075629T= , CM000676.2:g.65075629T= GRCh38
NC_000014.8:g.65542347T= , CM000676.1:g.65542347T= GRCh37
NC_000014.7:g.64612100T= NCBI36
NG_029830.1:g.31881A= , LRG_530:g.31881A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*847A= ENSP00000452206.2:n.*847A=
ENST00000556979.6:c.*1783A= ENSP00000452378.1:n.*1783A=
ENST00000358664.9:c.*847A= MANE Select ENSP00000351490.4:n.*847A=
ENST00000651648.1:c.145-5260A= ENSP00000498863.1:n.145-5260A=
ENST00000284165.10:c.*2174A= ENSP00000284165.6:n.*2174A=
ENST00000341653.6:c.171+18079A= ENSP00000342482.2:n.171+18079A=
ENST00000358402.8:c.*847A= ENSP00000351175.4:n.*847A=
ENST00000358664.8:c.*847A= ENSP00000351490.4:n.*847A=
ENST00000394606.6:c.*1103A= ENSP00000378104.2:n.*1103A=
ENST00000555932.5:c.*822A= ENSP00000450763.1:n.*822A=
ENST00000618858.4:c.*1119A= ENSP00000480127.1:n.*1119A=
NM_001271069.1:c.144+18079A= NP_001257998.1:n.144+18079A=
NM_002382.4:c.*847A= NP_002373.3:n.*847A=
NM_145112.2:c.*847A= NP_660087.1:n.*847A=
NM_145113.2:c.*1119A= NP_660088.1:n.*1119A=
NM_197957.3:c.171+18079A= NP_932061.1:n.171+18079A=
NR_073137.1:n.1454A=
XR_429315.2:n.1617A=
NM_001320415.1:c.*847A= NP_001307344.1:n.*847A=
XM_017021312.2:c.*847A= XP_016876801.1:n.*847A=
XM_017021313.1:c.*847A= XP_016876802.1:n.*847A=
XR_001750326.2:n.1675A=
XR_001750327.2:n.1594A=
XR_002957553.1:n.2108A=
XR_943450.3:n.1698A=
XR_943451.3:n.1714A=
XR_943452.3:n.1659A=
NM_001320415.2:c.*847A= NP_001307344.1:n.*847A=
NM_002382.5:c.*847A= MANE Select NP_002373.3:n.*847A=
NM_145112.3:c.*847A= NP_660087.1:n.*847A=
NM_145113.3:c.*1119A= NP_660088.1:n.*1119A=
NM_001271069.2:c.144+18079A= NP_001257998.1:n.144+18079A=
NM_197957.4:c.171+18079A= NP_932061.1:n.171+18079A=