Canonical Allele Identifier: CA390031293
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076515C>G , CM000676.2:g.65076515C>G GRCh38
NC_000014.8:g.65543233C>G , CM000676.1:g.65543233C>G GRCh37
NC_000014.7:g.64612986C>G NCBI36
NG_029830.1:g.30995G>C , LRG_530:g.30995G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.225G>C ENSP00000452206.2:p.Glu75Asp
ENST00000556979.6:c.*897G>C ENSP00000452378.1:n.*897G>C
ENST00000358664.9:c.444G>C MANE Select ENSP00000351490.4:p.Glu148Asp
ENST00000651648.1:c.145-6146G>C ENSP00000498863.1:n.145-6146G>C
ENST00000284165.10:c.*1288G>C ENSP00000284165.6:n.*1288G>C
ENST00000341653.6:c.171+17193G>C ENSP00000342482.2:n.171+17193G>C
ENST00000358402.8:c.417G>C ENSP00000351175.4:p.Glu139Asp
ENST00000358664.8:c.444G>C ENSP00000351490.4:p.Glu148Asp
ENST00000394606.6:c.*217G>C ENSP00000378104.2:n.*217G>C
ENST00000553928.5:c.*233G>C ENSP00000451907.1:n.*233G>C
ENST00000555419.5:c.336G>C ENSP00000452405.1:p.Glu112Asp
ENST00000555932.5:c.185G>C ENSP00000450763.1:p.Ser62Thr
ENST00000557277.5:c.255G>C ENSP00000450955.1:p.Glu85Asp
ENST00000618858.4:c.*233G>C ENSP00000480127.1:n.*233G>C
NM_001271069.1:c.144+17193G>C NP_001257998.1:n.144+17193G>C
NM_002382.4:c.444G>C NP_002373.3:p.Glu148Asp
NM_145112.2:c.417G>C NP_660087.1:p.Glu139Asp
NM_145113.2:c.*233G>C NP_660088.1:n.*233G>C
NM_197957.3:c.171+17193G>C NP_932061.1:n.171+17193G>C
NR_073137.1:n.568G>C
XR_429315.2:n.731G>C
NM_001320415.1:c.255G>C NP_001307344.1:p.Glu85Asp
XM_017021312.2:c.255G>C XP_016876801.1:p.Glu85Asp
XM_017021313.1:c.255G>C XP_016876802.1:p.Glu85Asp
XR_001750326.2:n.789G>C
XR_001750327.2:n.708G>C
XR_002957553.1:n.1222G>C
XR_943450.3:n.812G>C
XR_943451.3:n.828G>C
XR_943452.3:n.773G>C
NM_001320415.2:c.255G>C NP_001307344.1:p.Glu85Asp
NM_002382.5:c.444G>C MANE Select NP_002373.3:p.Glu148Asp
NM_145112.3:c.417G>C NP_660087.1:p.Glu139Asp
NM_145113.3:c.*233G>C NP_660088.1:n.*233G>C
NM_001271069.2:c.144+17193G>C NP_001257998.1:n.144+17193G>C
NM_197957.4:c.171+17193G>C NP_932061.1:n.171+17193G>C