Canonical Allele Identifier: CA2625289554
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076110G>T , CM000676.2:g.65076110G>T GRCh38
NC_000014.8:g.65542828G>T , CM000676.1:g.65542828G>T GRCh37
NC_000014.7:g.64612581G>T NCBI36
NG_029830.1:g.31400C>A , LRG_530:g.31400C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*366C>A ENSP00000452206.2:n.*366C>A
ENST00000556979.6:c.*1302C>A ENSP00000452378.1:n.*1302C>A
ENST00000358664.9:c.*366C>A MANE Select ENSP00000351490.4:n.*366C>A
ENST00000651648.1:c.145-5741C>A ENSP00000498863.1:n.145-5741C>A
ENST00000284165.10:c.*1693C>A ENSP00000284165.6:n.*1693C>A
ENST00000341653.6:c.171+17598C>A ENSP00000342482.2:n.171+17598C>A
ENST00000358402.8:c.*366C>A ENSP00000351175.4:n.*366C>A
ENST00000358664.8:c.*366C>A ENSP00000351490.4:n.*366C>A
ENST00000394606.6:c.*622C>A ENSP00000378104.2:n.*622C>A
ENST00000555419.5:c.741C>A ENSP00000452405.1:n.741C>A
ENST00000555932.5:c.*341C>A ENSP00000450763.1:n.*341C>A
ENST00000618858.4:c.*638C>A ENSP00000480127.1:n.*638C>A
NM_001271069.1:c.144+17598C>A NP_001257998.1:n.144+17598C>A
NM_002382.4:c.*366C>A NP_002373.3:n.*366C>A
NM_145112.2:c.*366C>A NP_660087.1:n.*366C>A
NM_145113.2:c.*638C>A NP_660088.1:n.*638C>A
NM_197957.3:c.171+17598C>A NP_932061.1:n.171+17598C>A
NR_073137.1:n.973C>A
XR_429315.2:n.1136C>A
NM_001320415.1:c.*366C>A NP_001307344.1:n.*366C>A
XM_017021312.2:c.*366C>A XP_016876801.1:n.*366C>A
XM_017021313.1:c.*366C>A XP_016876802.1:n.*366C>A
XR_001750326.2:n.1194C>A
XR_001750327.2:n.1113C>A
XR_002957553.1:n.1627C>A
XR_943450.3:n.1217C>A
XR_943451.3:n.1233C>A
XR_943452.3:n.1178C>A
NM_001320415.2:c.*366C>A NP_001307344.1:n.*366C>A
NM_002382.5:c.*366C>A MANE Select NP_002373.3:n.*366C>A
NM_145112.3:c.*366C>A NP_660087.1:n.*366C>A
NM_145113.3:c.*638C>A NP_660088.1:n.*638C>A
NM_001271069.2:c.144+17598C>A NP_001257998.1:n.144+17598C>A
NM_197957.4:c.171+17598C>A NP_932061.1:n.171+17598C>A