Canonical Allele Identifier: CA2142951201
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075640A= , CM000676.2:g.65075640A= GRCh38
NC_000014.8:g.65542358A= , CM000676.1:g.65542358A= GRCh37
NC_000014.7:g.64612111A= NCBI36
NG_029830.1:g.31870T= , LRG_530:g.31870T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*836T= ENSP00000452206.2:n.*836T=
ENST00000556979.6:c.*1772T= ENSP00000452378.1:n.*1772T=
ENST00000358664.9:c.*836T= MANE Select ENSP00000351490.4:n.*836T=
ENST00000651648.1:c.145-5271T= ENSP00000498863.1:n.145-5271T=
ENST00000284165.10:c.*2163T= ENSP00000284165.6:n.*2163T=
ENST00000341653.6:c.171+18068T= ENSP00000342482.2:n.171+18068T=
ENST00000358402.8:c.*836T= ENSP00000351175.4:n.*836T=
ENST00000358664.8:c.*836T= ENSP00000351490.4:n.*836T=
ENST00000394606.6:c.*1092T= ENSP00000378104.2:n.*1092T=
ENST00000555932.5:c.*811T= ENSP00000450763.1:n.*811T=
ENST00000618858.4:c.*1108T= ENSP00000480127.1:n.*1108T=
NM_001271069.1:c.144+18068T= NP_001257998.1:n.144+18068T=
NM_002382.4:c.*836T= NP_002373.3:n.*836T=
NM_145112.2:c.*836T= NP_660087.1:n.*836T=
NM_145113.2:c.*1108T= NP_660088.1:n.*1108T=
NM_197957.3:c.171+18068T= NP_932061.1:n.171+18068T=
NR_073137.1:n.1443T=
XR_429315.2:n.1606T=
NM_001320415.1:c.*836T= NP_001307344.1:n.*836T=
XM_017021312.2:c.*836T= XP_016876801.1:n.*836T=
XM_017021313.1:c.*836T= XP_016876802.1:n.*836T=
XR_001750326.2:n.1664T=
XR_001750327.2:n.1583T=
XR_002957553.1:n.2097T=
XR_943450.3:n.1687T=
XR_943451.3:n.1703T=
XR_943452.3:n.1648T=
NM_001320415.2:c.*836T= NP_001307344.1:n.*836T=
NM_002382.5:c.*836T= MANE Select NP_002373.3:n.*836T=
NM_145112.3:c.*836T= NP_660087.1:n.*836T=
NM_145113.3:c.*1108T= NP_660088.1:n.*1108T=
NM_001271069.2:c.144+18068T= NP_001257998.1:n.144+18068T=
NM_197957.4:c.171+18068T= NP_932061.1:n.171+18068T=