Canonical Allele Identifier: CA390031587
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076563A>G , CM000676.2:g.65076563A>G GRCh38
NC_000014.8:g.65543281A>G , CM000676.1:g.65543281A>G GRCh37
NC_000014.7:g.64613034A>G NCBI36
NG_029830.1:g.30947T>C , LRG_530:g.30947T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.177T>C ENSP00000452206.2:p.Ser59=
ENST00000556979.6:c.*849T>C ENSP00000452378.1:n.*849T>C
ENST00000358664.9:c.396T>C MANE Select ENSP00000351490.4:p.Ser132=
ENST00000651648.1:c.145-6194T>C ENSP00000498863.1:n.145-6194T>C
ENST00000284165.10:c.*1240T>C ENSP00000284165.6:n.*1240T>C
ENST00000341653.6:c.171+17145T>C ENSP00000342482.2:n.171+17145T>C
ENST00000358402.8:c.369T>C ENSP00000351175.4:p.Ser123=
ENST00000358664.8:c.396T>C ENSP00000351490.4:p.Ser132=
ENST00000394606.6:c.*169T>C ENSP00000378104.2:n.*169T>C
ENST00000553928.5:c.*185T>C ENSP00000451907.1:n.*185T>C
ENST00000555419.5:c.288T>C ENSP00000452405.1:p.Ser96=
ENST00000555932.5:c.137T>C ENSP00000450763.1:p.Leu46Pro
ENST00000557277.5:c.207T>C ENSP00000450955.1:p.Ser69=
ENST00000618858.4:c.*185T>C ENSP00000480127.1:n.*185T>C
NM_001271069.1:c.144+17145T>C NP_001257998.1:n.144+17145T>C
NM_002382.4:c.396T>C NP_002373.3:p.Ser132=
NM_145112.2:c.369T>C NP_660087.1:p.Ser123=
NM_145113.2:c.*185T>C NP_660088.1:n.*185T>C
NM_197957.3:c.171+17145T>C NP_932061.1:n.171+17145T>C
NR_073137.1:n.520T>C
XR_429315.2:n.683T>C
NM_001320415.1:c.207T>C NP_001307344.1:p.Ser69=
XM_017021312.2:c.207T>C XP_016876801.1:p.Ser69=
XM_017021313.1:c.207T>C XP_016876802.1:p.Ser69=
XR_001750326.2:n.741T>C
XR_001750327.2:n.660T>C
XR_002957553.1:n.1174T>C
XR_943450.3:n.764T>C
XR_943451.3:n.780T>C
XR_943452.3:n.725T>C
NM_001320415.2:c.207T>C NP_001307344.1:p.Ser69=
NM_002382.5:c.396T>C MANE Select NP_002373.3:p.Ser132=
NM_145112.3:c.369T>C NP_660087.1:p.Ser123=
NM_145113.3:c.*185T>C NP_660088.1:n.*185T>C
NM_001271069.2:c.144+17145T>C NP_001257998.1:n.144+17145T>C
NM_197957.4:c.171+17145T>C NP_932061.1:n.171+17145T>C