Canonical Allele Identifier: CA262717089
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 568216
dbSNP Id: rs201312694

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076556C>G , CM000676.2:g.65076556C>G GRCh38
NC_000014.8:g.65543274C>G , CM000676.1:g.65543274C>G GRCh37
NC_000014.7:g.64613027C>G NCBI36
NG_029830.1:g.30954G>C , LRG_530:g.30954G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.184G>C ENSP00000452206.2:p.Asp62His
ENST00000556979.6:c.*856G>C ENSP00000452378.1:n.*856G>C
ENST00000358664.9:c.403G>C MANE Select ENSP00000351490.4:p.Asp135His
ENST00000651648.1:c.145-6187G>C ENSP00000498863.1:n.145-6187G>C
ENST00000284165.10:c.*1247G>C ENSP00000284165.6:n.*1247G>C
ENST00000341653.6:c.171+17152G>C ENSP00000342482.2:n.171+17152G>C
ENST00000358402.8:c.376G>C ENSP00000351175.4:p.Asp126His
ENST00000358664.8:c.403G>C ENSP00000351490.4:p.Asp135His
ENST00000394606.6:c.*176G>C ENSP00000378104.2:n.*176G>C
ENST00000553928.5:c.*192G>C ENSP00000451907.1:n.*192G>C
ENST00000555419.5:c.295G>C ENSP00000452405.1:p.Asp99His
ENST00000555932.5:c.144G>C ENSP00000450763.1:p.Ser48=
ENST00000557277.5:c.214G>C ENSP00000450955.1:p.Asp72His
ENST00000618858.4:c.*192G>C ENSP00000480127.1:n.*192G>C
NM_001271069.1:c.144+17152G>C NP_001257998.1:n.144+17152G>C
NM_002382.4:c.403G>C NP_002373.3:p.Asp135His
NM_145112.2:c.376G>C NP_660087.1:p.Asp126His
NM_145113.2:c.*192G>C NP_660088.1:n.*192G>C
NM_197957.3:c.171+17152G>C NP_932061.1:n.171+17152G>C
NR_073137.1:n.527G>C
XR_429315.2:n.690G>C
NM_001320415.1:c.214G>C NP_001307344.1:p.Asp72His
XM_017021312.2:c.214G>C XP_016876801.1:p.Asp72His
XM_017021313.1:c.214G>C XP_016876802.1:p.Asp72His
XR_001750326.2:n.748G>C
XR_001750327.2:n.667G>C
XR_002957553.1:n.1181G>C
XR_943450.3:n.771G>C
XR_943451.3:n.787G>C
XR_943452.3:n.732G>C
NM_001320415.2:c.214G>C NP_001307344.1:p.Asp72His
NM_002382.5:c.403G>C MANE Select NP_002373.3:p.Asp135His
NM_145112.3:c.376G>C NP_660087.1:p.Asp126His
NM_145113.3:c.*192G>C NP_660088.1:n.*192G>C
NM_001271069.2:c.144+17152G>C NP_001257998.1:n.144+17152G>C
NM_197957.4:c.171+17152G>C NP_932061.1:n.171+17152G>C