Canonical Allele Identifier: CA2142951193
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075616T= , CM000676.2:g.65075616T= GRCh38
NC_000014.8:g.65542334T= , CM000676.1:g.65542334T= GRCh37
NC_000014.7:g.64612087T= NCBI36
NG_029830.1:g.31894A= , LRG_530:g.31894A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*860A= ENSP00000452206.2:n.*860A=
ENST00000556979.6:c.*1796A= ENSP00000452378.1:n.*1796A=
ENST00000358664.9:c.*860A= MANE Select ENSP00000351490.4:n.*860A=
ENST00000651648.1:c.145-5247A= ENSP00000498863.1:n.145-5247A=
ENST00000284165.10:c.*2187A= ENSP00000284165.6:n.*2187A=
ENST00000341653.6:c.171+18092A= ENSP00000342482.2:n.171+18092A=
ENST00000358402.8:c.*860A= ENSP00000351175.4:n.*860A=
ENST00000358664.8:c.*860A= ENSP00000351490.4:n.*860A=
ENST00000394606.6:c.*1116A= ENSP00000378104.2:n.*1116A=
ENST00000555932.5:c.*835A= ENSP00000450763.1:n.*835A=
ENST00000618858.4:c.*1132A= ENSP00000480127.1:n.*1132A=
NM_001271069.1:c.144+18092A= NP_001257998.1:n.144+18092A=
NM_002382.4:c.*860A= NP_002373.3:n.*860A=
NM_145112.2:c.*860A= NP_660087.1:n.*860A=
NM_145113.2:c.*1132A= NP_660088.1:n.*1132A=
NM_197957.3:c.171+18092A= NP_932061.1:n.171+18092A=
NR_073137.1:n.1467A=
XR_429315.2:n.1630A=
NM_001320415.1:c.*860A= NP_001307344.1:n.*860A=
XM_017021312.2:c.*860A= XP_016876801.1:n.*860A=
XM_017021313.1:c.*860A= XP_016876802.1:n.*860A=
XR_001750326.2:n.1688A=
XR_001750327.2:n.1607A=
XR_002957553.1:n.2121A=
XR_943450.3:n.1711A=
XR_943451.3:n.1727A=
XR_943452.3:n.1672A=
NM_001320415.2:c.*860A= NP_001307344.1:n.*860A=
NM_002382.5:c.*860A= MANE Select NP_002373.3:n.*860A=
NM_145112.3:c.*860A= NP_660087.1:n.*860A=
NM_145113.3:c.*1132A= NP_660088.1:n.*1132A=
NM_001271069.2:c.144+18092A= NP_001257998.1:n.144+18092A=
NM_197957.4:c.171+18092A= NP_932061.1:n.171+18092A=