Canonical Allele Identifier: CA614736756
Gene: MAX HGNC NCBI

Linked Data

dbSNP Id: rs1402574606

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076448T>C , CM000676.2:g.65076448T>C GRCh38
NC_000014.8:g.65543166T>C , CM000676.1:g.65543166T>C GRCh37
NC_000014.7:g.64612919T>C NCBI36
NG_029830.1:g.31062A>G , LRG_530:g.31062A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*28A>G ENSP00000452206.2:n.*28A>G
ENST00000556979.6:c.*964A>G ENSP00000452378.1:n.*964A>G
ENST00000358664.9:c.*28A>G MANE Select ENSP00000351490.4:n.*28A>G
ENST00000651648.1:c.145-6079A>G ENSP00000498863.1:n.145-6079A>G
ENST00000284165.10:c.*1355A>G ENSP00000284165.6:n.*1355A>G
ENST00000341653.6:c.171+17260A>G ENSP00000342482.2:n.171+17260A>G
ENST00000358402.8:c.*28A>G ENSP00000351175.4:n.*28A>G
ENST00000358664.8:c.*28A>G ENSP00000351490.4:n.*28A>G
ENST00000394606.6:c.*284A>G ENSP00000378104.2:n.*284A>G
ENST00000555419.5:c.403A>G ENSP00000452405.1:n.403A>G
ENST00000555932.5:c.*3A>G ENSP00000450763.1:n.*3A>G
ENST00000618858.4:c.*300A>G ENSP00000480127.1:n.*300A>G
NM_001271069.1:c.144+17260A>G NP_001257998.1:n.144+17260A>G
NM_002382.4:c.*28A>G NP_002373.3:n.*28A>G
NM_145112.2:c.*28A>G NP_660087.1:n.*28A>G
NM_145113.2:c.*300A>G NP_660088.1:n.*300A>G
NM_197957.3:c.171+17260A>G NP_932061.1:n.171+17260A>G
NR_073137.1:n.635A>G
XR_429315.2:n.798A>G
NM_001320415.1:c.*28A>G NP_001307344.1:n.*28A>G
XM_017021312.2:c.*28A>G XP_016876801.1:n.*28A>G
XM_017021313.1:c.*28A>G XP_016876802.1:n.*28A>G
XR_001750326.2:n.856A>G
XR_001750327.2:n.775A>G
XR_002957553.1:n.1289A>G
XR_943450.3:n.879A>G
XR_943451.3:n.895A>G
XR_943452.3:n.840A>G
NM_001320415.2:c.*28A>G NP_001307344.1:n.*28A>G
NM_002382.5:c.*28A>G MANE Select NP_002373.3:n.*28A>G
NM_145112.3:c.*28A>G NP_660087.1:n.*28A>G
NM_145113.3:c.*300A>G NP_660088.1:n.*300A>G
NM_001271069.2:c.144+17260A>G NP_001257998.1:n.144+17260A>G
NM_197957.4:c.171+17260A>G NP_932061.1:n.171+17260A>G