Canonical Allele Identifier: CA1139770500
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076088del , CM000676.2:g.65076088del GRCh38
NC_000014.8:g.65542806del , CM000676.1:g.65542806del GRCh37
NC_000014.7:g.64612559del NCBI36
NG_029830.1:g.31422del , LRG_530:g.31422del

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*388del ENSP00000452206.2:n.*388del
ENST00000556979.6:c.*1324del ENSP00000452378.1:n.*1324del
ENST00000358664.9:c.*388del MANE Select ENSP00000351490.4:n.*388del
ENST00000651648.1:c.145-5719del ENSP00000498863.1:n.145-5719del
ENST00000284165.10:c.*1715del ENSP00000284165.6:n.*1715del
ENST00000341653.6:c.171+17620del ENSP00000342482.2:n.171+17620del
ENST00000358402.8:c.*388del ENSP00000351175.4:n.*388del
ENST00000358664.8:c.*388del ENSP00000351490.4:n.*388del
ENST00000394606.6:c.*644del ENSP00000378104.2:n.*644del
ENST00000555419.5:c.763del ENSP00000452405.1:n.763del
ENST00000555932.5:c.*363del ENSP00000450763.1:n.*363del
ENST00000618858.4:c.*660del ENSP00000480127.1:n.*660del
NM_001271069.1:c.144+17620del NP_001257998.1:n.144+17620del
NM_002382.4:c.*388del NP_002373.3:n.*388del
NM_145112.2:c.*388del NP_660087.1:n.*388del
NM_145113.2:c.*660del NP_660088.1:n.*660del
NM_197957.3:c.171+17620del NP_932061.1:n.171+17620del
NR_073137.1:n.995del
XR_429315.2:n.1158del
NM_001320415.1:c.*388del NP_001307344.1:n.*388del
XM_017021312.2:c.*388del XP_016876801.1:n.*388del
XM_017021313.1:c.*388del XP_016876802.1:n.*388del
XR_001750326.2:n.1216del
XR_001750327.2:n.1135del
XR_002957553.1:n.1649del
XR_943450.3:n.1239del
XR_943451.3:n.1255del
XR_943452.3:n.1200del
NM_001320415.2:c.*388del NP_001307344.1:n.*388del
NM_002382.5:c.*388del MANE Select NP_002373.3:n.*388del
NM_145112.3:c.*388del NP_660087.1:n.*388del
NM_145113.3:c.*660del NP_660088.1:n.*660del
NM_001271069.2:c.144+17620del NP_001257998.1:n.144+17620del
NM_197957.4:c.171+17620del NP_932061.1:n.171+17620del