Canonical Allele Identifier: CA390031379
Gene: MAX HGNC NCBI

Linked Data

dbSNP Id: rs2139739766

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076529A>C , CM000676.2:g.65076529A>C GRCh38
NC_000014.8:g.65543247A>C , CM000676.1:g.65543247A>C GRCh37
NC_000014.7:g.64613000A>C NCBI36
NG_029830.1:g.30981T>G , LRG_530:g.30981T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.211T>G ENSP00000452206.2:p.Ser71Ala
ENST00000556979.6:c.*883T>G ENSP00000452378.1:n.*883T>G
ENST00000358664.9:c.430T>G MANE Select ENSP00000351490.4:p.Ser144Ala
ENST00000651648.1:c.145-6160T>G ENSP00000498863.1:n.145-6160T>G
ENST00000284165.10:c.*1274T>G ENSP00000284165.6:n.*1274T>G
ENST00000341653.6:c.171+17179T>G ENSP00000342482.2:n.171+17179T>G
ENST00000358402.8:c.403T>G ENSP00000351175.4:p.Ser135Ala
ENST00000358664.8:c.430T>G ENSP00000351490.4:p.Ser144Ala
ENST00000394606.6:c.*203T>G ENSP00000378104.2:n.*203T>G
ENST00000553928.5:c.*219T>G ENSP00000451907.1:n.*219T>G
ENST00000555419.5:c.322T>G ENSP00000452405.1:p.Ser108Ala
ENST00000555932.5:c.171T>G ENSP00000450763.1:p.Ser57Arg
ENST00000557277.5:c.241T>G ENSP00000450955.1:p.Ser81Ala
ENST00000618858.4:c.*219T>G ENSP00000480127.1:n.*219T>G
NM_001271069.1:c.144+17179T>G NP_001257998.1:n.144+17179T>G
NM_002382.4:c.430T>G NP_002373.3:p.Ser144Ala
NM_145112.2:c.403T>G NP_660087.1:p.Ser135Ala
NM_145113.2:c.*219T>G NP_660088.1:n.*219T>G
NM_197957.3:c.171+17179T>G NP_932061.1:n.171+17179T>G
NR_073137.1:n.554T>G
XR_429315.2:n.717T>G
NM_001320415.1:c.241T>G NP_001307344.1:p.Ser81Ala
XM_017021312.2:c.241T>G XP_016876801.1:p.Ser81Ala
XM_017021313.1:c.241T>G XP_016876802.1:p.Ser81Ala
XR_001750326.2:n.775T>G
XR_001750327.2:n.694T>G
XR_002957553.1:n.1208T>G
XR_943450.3:n.798T>G
XR_943451.3:n.814T>G
XR_943452.3:n.759T>G
NM_001320415.2:c.241T>G NP_001307344.1:p.Ser81Ala
NM_002382.5:c.430T>G MANE Select NP_002373.3:p.Ser144Ala
NM_145112.3:c.403T>G NP_660087.1:p.Ser135Ala
NM_145113.3:c.*219T>G NP_660088.1:n.*219T>G
NM_001271069.2:c.144+17179T>G NP_001257998.1:n.144+17179T>G
NM_197957.4:c.171+17179T>G NP_932061.1:n.171+17179T>G