Canonical Allele Identifier: CA2625289552
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076111dup , CM000676.2:g.65076111dup GRCh38
NC_000014.8:g.65542829dup , CM000676.1:g.65542829dup GRCh37
NC_000014.7:g.64612582dup NCBI36
NG_029830.1:g.31401dup , LRG_530:g.31401dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*367dup ENSP00000452206.2:n.*367dup
ENST00000556979.6:c.*1303dup ENSP00000452378.1:n.*1303dup
ENST00000358664.9:c.*367dup MANE Select ENSP00000351490.4:n.*367dup
ENST00000651648.1:c.145-5740dup ENSP00000498863.1:n.145-5740dup
ENST00000284165.10:c.*1694dup ENSP00000284165.6:n.*1694dup
ENST00000341653.6:c.171+17599dup ENSP00000342482.2:n.171+17599dup
ENST00000358402.8:c.*367dup ENSP00000351175.4:n.*367dup
ENST00000358664.8:c.*367dup ENSP00000351490.4:n.*367dup
ENST00000394606.6:c.*623dup ENSP00000378104.2:n.*623dup
ENST00000555419.5:c.742dup ENSP00000452405.1:n.742dup
ENST00000555932.5:c.*342dup ENSP00000450763.1:n.*342dup
ENST00000618858.4:c.*639dup ENSP00000480127.1:n.*639dup
NM_001271069.1:c.144+17599dup NP_001257998.1:n.144+17599dup
NM_002382.4:c.*367dup NP_002373.3:n.*367dup
NM_145112.2:c.*367dup NP_660087.1:n.*367dup
NM_145113.2:c.*639dup NP_660088.1:n.*639dup
NM_197957.3:c.171+17599dup NP_932061.1:n.171+17599dup
NR_073137.1:n.974dup
XR_429315.2:n.1137dup
NM_001320415.1:c.*367dup NP_001307344.1:n.*367dup
XM_017021312.2:c.*367dup XP_016876801.1:n.*367dup
XM_017021313.1:c.*367dup XP_016876802.1:n.*367dup
XR_001750326.2:n.1195dup
XR_001750327.2:n.1114dup
XR_002957553.1:n.1628dup
XR_943450.3:n.1218dup
XR_943451.3:n.1234dup
XR_943452.3:n.1179dup
NM_001320415.2:c.*367dup NP_001307344.1:n.*367dup
NM_002382.5:c.*367dup MANE Select NP_002373.3:n.*367dup
NM_145112.3:c.*367dup NP_660087.1:n.*367dup
NM_145113.3:c.*639dup NP_660088.1:n.*639dup
NM_001271069.2:c.144+17599dup NP_001257998.1:n.144+17599dup
NM_197957.4:c.171+17599dup NP_932061.1:n.171+17599dup