Canonical Allele Identifier: CA390031681
Gene: MAX HGNC NCBI

Linked Data

dbSNP Id: rs2139740561

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076576C>T , CM000676.2:g.65076576C>T GRCh38
NC_000014.8:g.65543294C>T , CM000676.1:g.65543294C>T GRCh37
NC_000014.7:g.64613047C>T NCBI36
NG_029830.1:g.30934G>A , LRG_530:g.30934G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.164G>A ENSP00000452206.2:p.Gly55Asp
ENST00000556979.6:c.*836G>A ENSP00000452378.1:n.*836G>A
ENST00000358664.9:c.383G>A MANE Select ENSP00000351490.4:p.Gly128Asp
ENST00000651648.1:c.145-6207G>A ENSP00000498863.1:n.145-6207G>A
ENST00000284165.10:c.*1227G>A ENSP00000284165.6:n.*1227G>A
ENST00000341653.6:c.171+17132G>A ENSP00000342482.2:n.171+17132G>A
ENST00000358402.8:c.356G>A ENSP00000351175.4:p.Gly119Asp
ENST00000358664.8:c.383G>A ENSP00000351490.4:p.Gly128Asp
ENST00000394606.6:c.*156G>A ENSP00000378104.2:n.*156G>A
ENST00000553928.5:c.*172G>A ENSP00000451907.1:n.*172G>A
ENST00000555419.5:c.275G>A ENSP00000452405.1:p.Gly92Asp
ENST00000555932.5:c.124G>A ENSP00000450763.1:p.Ala42Thr
ENST00000557277.5:c.194G>A ENSP00000450955.1:p.Gly65Asp
ENST00000618858.4:c.*172G>A ENSP00000480127.1:n.*172G>A
NM_001271069.1:c.144+17132G>A NP_001257998.1:n.144+17132G>A
NM_002382.4:c.383G>A NP_002373.3:p.Gly128Asp
NM_145112.2:c.356G>A NP_660087.1:p.Gly119Asp
NM_145113.2:c.*172G>A NP_660088.1:n.*172G>A
NM_197957.3:c.171+17132G>A NP_932061.1:n.171+17132G>A
NR_073137.1:n.507G>A
XR_429315.2:n.670G>A
XR_943451.1:n.767G>A
NM_001320415.1:c.194G>A NP_001307344.1:p.Gly65Asp
XM_017021312.2:c.194G>A XP_016876801.1:p.Gly65Asp
XM_017021313.1:c.194G>A XP_016876802.1:p.Gly65Asp
XR_001750326.2:n.728G>A
XR_001750327.2:n.647G>A
XR_002957553.1:n.1161G>A
XR_943450.3:n.751G>A
XR_943451.3:n.767G>A
XR_943452.3:n.712G>A
NM_001320415.2:c.194G>A NP_001307344.1:p.Gly65Asp
NM_002382.5:c.383G>A MANE Select NP_002373.3:p.Gly128Asp
NM_145112.3:c.356G>A NP_660087.1:p.Gly119Asp
NM_145113.3:c.*172G>A NP_660088.1:n.*172G>A
NM_001271069.2:c.144+17132G>A NP_001257998.1:n.144+17132G>A
NM_197957.4:c.171+17132G>A NP_932061.1:n.171+17132G>A