Canonical Allele Identifier: CA707784626
Gene: MAX HGNC NCBI

Linked Data

dbSNP Id: rs1181169009

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075994T>C , CM000676.2:g.65075994T>C GRCh38
NC_000014.8:g.65542712T>C , CM000676.1:g.65542712T>C GRCh37
NC_000014.7:g.64612465T>C NCBI36
NG_029830.1:g.31516A>G , LRG_530:g.31516A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*482A>G ENSP00000452206.2:n.*482A>G
ENST00000556979.6:c.*1418A>G ENSP00000452378.1:n.*1418A>G
ENST00000358664.9:c.*482A>G MANE Select ENSP00000351490.4:n.*482A>G
ENST00000651648.1:c.145-5625A>G ENSP00000498863.1:n.145-5625A>G
ENST00000284165.10:c.*1809A>G ENSP00000284165.6:n.*1809A>G
ENST00000341653.6:c.171+17714A>G ENSP00000342482.2:n.171+17714A>G
ENST00000358402.8:c.*482A>G ENSP00000351175.4:n.*482A>G
ENST00000358664.8:c.*482A>G ENSP00000351490.4:n.*482A>G
ENST00000394606.6:c.*738A>G ENSP00000378104.2:n.*738A>G
ENST00000555932.5:c.*457A>G ENSP00000450763.1:n.*457A>G
ENST00000618858.4:c.*754A>G ENSP00000480127.1:n.*754A>G
NM_001271069.1:c.144+17714A>G NP_001257998.1:n.144+17714A>G
NM_002382.4:c.*482A>G NP_002373.3:n.*482A>G
NM_145112.2:c.*482A>G NP_660087.1:n.*482A>G
NM_145113.2:c.*754A>G NP_660088.1:n.*754A>G
NM_197957.3:c.171+17714A>G NP_932061.1:n.171+17714A>G
NR_073137.1:n.1089A>G
XR_429315.2:n.1252A>G
NM_001320415.1:c.*482A>G NP_001307344.1:n.*482A>G
XM_017021312.2:c.*482A>G XP_016876801.1:n.*482A>G
XM_017021313.1:c.*482A>G XP_016876802.1:n.*482A>G
XR_001750326.2:n.1310A>G
XR_001750327.2:n.1229A>G
XR_002957553.1:n.1743A>G
XR_943450.3:n.1333A>G
XR_943451.3:n.1349A>G
XR_943452.3:n.1294A>G
NM_001320415.2:c.*482A>G NP_001307344.1:n.*482A>G
NM_002382.5:c.*482A>G MANE Select NP_002373.3:n.*482A>G
NM_145112.3:c.*482A>G NP_660087.1:n.*482A>G
NM_145113.3:c.*754A>G NP_660088.1:n.*754A>G
NM_001271069.2:c.144+17714A>G NP_001257998.1:n.144+17714A>G
NM_197957.4:c.171+17714A>G NP_932061.1:n.171+17714A>G