Canonical Allele Identifier: CA390031828
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076612G>C , CM000676.2:g.65076612G>C GRCh38
NC_000014.8:g.65543330G>C , CM000676.1:g.65543330G>C GRCh37
NC_000014.7:g.64613083G>C NCBI36
NG_029830.1:g.30898C>G , LRG_530:g.30898C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.128C>G ENSP00000452206.2:p.Pro43Arg
ENST00000556979.6:c.*800C>G ENSP00000452378.1:n.*800C>G
ENST00000358664.9:c.347C>G MANE Select ENSP00000351490.4:p.Pro116Arg
ENST00000651648.1:c.145-6243C>G ENSP00000498863.1:n.145-6243C>G
ENST00000284165.10:c.*1191C>G ENSP00000284165.6:n.*1191C>G
ENST00000341653.6:c.171+17096C>G ENSP00000342482.2:n.171+17096C>G
ENST00000358402.8:c.320C>G ENSP00000351175.4:p.Pro107Arg
ENST00000358664.8:c.347C>G ENSP00000351490.4:p.Pro116Arg
ENST00000394606.6:c.*120C>G ENSP00000378104.2:n.*120C>G
ENST00000553928.5:c.*136C>G ENSP00000451907.1:n.*136C>G
ENST00000555419.5:c.239C>G ENSP00000452405.1:p.Pro80Arg
ENST00000555932.5:c.88C>G ENSP00000450763.1:p.Pro30Ala
ENST00000556892.5:c.128C>G ENSP00000452206.1:p.Pro43Arg
ENST00000557277.5:c.158C>G ENSP00000450955.1:p.Pro53Arg
ENST00000618858.4:c.*136C>G ENSP00000480127.1:n.*136C>G
NM_001271069.1:c.144+17096C>G NP_001257998.1:n.144+17096C>G
NM_002382.4:c.347C>G NP_002373.3:p.Pro116Arg
NM_145112.2:c.320C>G NP_660087.1:p.Pro107Arg
NM_145113.2:c.*136C>G NP_660088.1:n.*136C>G
NM_197957.3:c.171+17096C>G NP_932061.1:n.171+17096C>G
NR_073137.1:n.471C>G
XR_429315.2:n.634C>G
XR_943450.1:n.715C>G
XR_943451.1:n.731C>G
XR_943452.1:n.677C>G
NM_001320415.1:c.158C>G NP_001307344.1:p.Pro53Arg
XM_017021312.2:c.158C>G XP_016876801.1:p.Pro53Arg
XM_017021313.1:c.158C>G XP_016876802.1:p.Pro53Arg
XR_001750326.2:n.692C>G
XR_001750327.2:n.611C>G
XR_002957553.1:n.1125C>G
XR_943450.3:n.715C>G
XR_943451.3:n.731C>G
XR_943452.3:n.676C>G
NM_001320415.2:c.158C>G NP_001307344.1:p.Pro53Arg
NM_002382.5:c.347C>G MANE Select NP_002373.3:p.Pro116Arg
NM_145112.3:c.320C>G NP_660087.1:p.Pro107Arg
NM_145113.3:c.*136C>G NP_660088.1:n.*136C>G
NM_001271069.2:c.144+17096C>G NP_001257998.1:n.144+17096C>G
NM_197957.4:c.171+17096C>G NP_932061.1:n.171+17096C>G