Canonical Allele Identifier: CA390031820
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076609G>C , CM000676.2:g.65076609G>C GRCh38
NC_000014.8:g.65543327G>C , CM000676.1:g.65543327G>C GRCh37
NC_000014.7:g.64613080G>C NCBI36
NG_029830.1:g.30901C>G , LRG_530:g.30901C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.131C>G ENSP00000452206.2:p.Ser44Cys
ENST00000556979.6:c.*803C>G ENSP00000452378.1:n.*803C>G
ENST00000358664.9:c.350C>G MANE Select ENSP00000351490.4:p.Ser117Cys
ENST00000651648.1:c.145-6240C>G ENSP00000498863.1:n.145-6240C>G
ENST00000284165.10:c.*1194C>G ENSP00000284165.6:n.*1194C>G
ENST00000341653.6:c.171+17099C>G ENSP00000342482.2:n.171+17099C>G
ENST00000358402.8:c.323C>G ENSP00000351175.4:p.Ser108Cys
ENST00000358664.8:c.350C>G ENSP00000351490.4:p.Ser117Cys
ENST00000394606.6:c.*123C>G ENSP00000378104.2:n.*123C>G
ENST00000553928.5:c.*139C>G ENSP00000451907.1:n.*139C>G
ENST00000555419.5:c.242C>G ENSP00000452405.1:p.Ser81Cys
ENST00000555932.5:c.91C>G ENSP00000450763.1:p.Pro31Ala
ENST00000556892.5:c.131C>G
ENST00000557277.5:c.161C>G ENSP00000450955.1:p.Ser54Cys
ENST00000618858.4:c.*139C>G ENSP00000480127.1:n.*139C>G
NM_001271069.1:c.144+17099C>G NP_001257998.1:n.144+17099C>G
NM_002382.4:c.350C>G NP_002373.3:p.Ser117Cys
NM_145112.2:c.323C>G NP_660087.1:p.Ser108Cys
NM_145113.2:c.*139C>G NP_660088.1:n.*139C>G
NM_197957.3:c.171+17099C>G NP_932061.1:n.171+17099C>G
NR_073137.1:n.474C>G
XR_429315.2:n.637C>G
XR_943450.1:n.718C>G
XR_943451.1:n.734C>G
XR_943452.1:n.680C>G
NM_001320415.1:c.161C>G NP_001307344.1:p.Ser54Cys
XM_017021312.2:c.161C>G XP_016876801.1:p.Ser54Cys
XM_017021313.1:c.161C>G XP_016876802.1:p.Ser54Cys
XR_001750326.2:n.695C>G
XR_001750327.2:n.614C>G
XR_002957553.1:n.1128C>G
XR_943450.3:n.718C>G
XR_943451.3:n.734C>G
XR_943452.3:n.679C>G
NM_001320415.2:c.161C>G NP_001307344.1:p.Ser54Cys
NM_002382.5:c.350C>G MANE Select NP_002373.3:p.Ser117Cys
NM_145112.3:c.323C>G NP_660087.1:p.Ser108Cys
NM_145113.3:c.*139C>G NP_660088.1:n.*139C>G
NM_001271069.2:c.144+17099C>G NP_001257998.1:n.144+17099C>G
NM_197957.4:c.171+17099C>G NP_932061.1:n.171+17099C>G