Canonical Allele Identifier: CA390031564
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076560G>C , CM000676.2:g.65076560G>C GRCh38
NC_000014.8:g.65543278G>C , CM000676.1:g.65543278G>C GRCh37
NC_000014.7:g.64613031G>C NCBI36
NG_029830.1:g.30950C>G , LRG_530:g.30950C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.180C>G ENSP00000452206.2:p.Ala60=
ENST00000556979.6:c.*852C>G ENSP00000452378.1:n.*852C>G
ENST00000358664.9:c.399C>G MANE Select ENSP00000351490.4:p.Ala133=
ENST00000651648.1:c.145-6191C>G ENSP00000498863.1:n.145-6191C>G
ENST00000284165.10:c.*1243C>G ENSP00000284165.6:n.*1243C>G
ENST00000341653.6:c.171+17148C>G ENSP00000342482.2:n.171+17148C>G
ENST00000358402.8:c.372C>G ENSP00000351175.4:p.Ala124=
ENST00000358664.8:c.399C>G ENSP00000351490.4:p.Ala133=
ENST00000394606.6:c.*172C>G ENSP00000378104.2:n.*172C>G
ENST00000553928.5:c.*188C>G ENSP00000451907.1:n.*188C>G
ENST00000555419.5:c.291C>G ENSP00000452405.1:p.Ala97=
ENST00000555932.5:c.140C>G ENSP00000450763.1:p.Pro47Arg
ENST00000557277.5:c.210C>G ENSP00000450955.1:p.Ala70=
ENST00000618858.4:c.*188C>G ENSP00000480127.1:n.*188C>G
NM_001271069.1:c.144+17148C>G NP_001257998.1:n.144+17148C>G
NM_002382.4:c.399C>G NP_002373.3:p.Ala133=
NM_145112.2:c.372C>G NP_660087.1:p.Ala124=
NM_145113.2:c.*188C>G NP_660088.1:n.*188C>G
NM_197957.3:c.171+17148C>G NP_932061.1:n.171+17148C>G
NR_073137.1:n.523C>G
XR_429315.2:n.686C>G
NM_001320415.1:c.210C>G NP_001307344.1:p.Ala70=
XM_017021312.2:c.210C>G XP_016876801.1:p.Ala70=
XM_017021313.1:c.210C>G XP_016876802.1:p.Ala70=
XR_001750326.2:n.744C>G
XR_001750327.2:n.663C>G
XR_002957553.1:n.1177C>G
XR_943450.3:n.767C>G
XR_943451.3:n.783C>G
XR_943452.3:n.728C>G
NM_001320415.2:c.210C>G NP_001307344.1:p.Ala70=
NM_002382.5:c.399C>G MANE Select NP_002373.3:p.Ala133=
NM_145112.3:c.372C>G NP_660087.1:p.Ala124=
NM_145113.3:c.*188C>G NP_660088.1:n.*188C>G
NM_001271069.2:c.144+17148C>G NP_001257998.1:n.144+17148C>G
NM_197957.4:c.171+17148C>G NP_932061.1:n.171+17148C>G