Canonical Allele Identifier: CA2142951307
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075833A= , CM000676.2:g.65075833A= GRCh38
NC_000014.8:g.65542551A= , CM000676.1:g.65542551A= GRCh37
NC_000014.7:g.64612304A= NCBI36
NG_029830.1:g.31677T= , LRG_530:g.31677T=

Transcript Alleles

HGVS Amino-acid change
ENST00000556892.6:c.*643T= ENSP00000452206.2:n.*643T=
ENST00000556979.6:c.*1579T= ENSP00000452378.1:n.*1579T=
ENST00000358664.9:c.*643T= MANE Select ENSP00000351490.4:n.*643T=
ENST00000651648.1:c.145-5464T= ENSP00000498863.1:n.145-5464T=
ENST00000284165.10:c.*1970T= ENSP00000284165.6:n.*1970T=
ENST00000341653.6:c.171+17875T= ENSP00000342482.2:n.171+17875T=
ENST00000358402.8:c.*643T= ENSP00000351175.4:n.*643T=
ENST00000358664.8:c.*643T= ENSP00000351490.4:n.*643T=
ENST00000394606.6:c.*899T= ENSP00000378104.2:n.*899T=
ENST00000555932.5:c.*618T= ENSP00000450763.1:n.*618T=
ENST00000618858.4:c.*915T= ENSP00000480127.1:n.*915T=
NM_001271069.1:c.144+17875T= NP_001257998.1:n.144+17875T=
NM_002382.4:c.*643T= NP_002373.3:n.*643T=
NM_145112.2:c.*643T= NP_660087.1:n.*643T=
NM_145113.2:c.*915T= NP_660088.1:n.*915T=
NM_197957.3:c.171+17875T= NP_932061.1:n.171+17875T=
NR_073137.1:n.1250T=
XR_429315.2:n.1413T=
NM_001320415.1:c.*643T= NP_001307344.1:n.*643T=
XM_017021312.2:c.*643T= XP_016876801.1:n.*643T=
XM_017021313.1:c.*643T= XP_016876802.1:n.*643T=
XR_001750326.2:n.1471T=
XR_001750327.2:n.1390T=
XR_002957553.1:n.1904T=
XR_943450.3:n.1494T=
XR_943451.3:n.1510T=
XR_943452.3:n.1455T=
NM_001320415.2:c.*643T= NP_001307344.1:n.*643T=
NM_002382.5:c.*643T= MANE Select NP_002373.3:n.*643T=
NM_145112.3:c.*643T= NP_660087.1:n.*643T=
NM_145113.3:c.*915T= NP_660088.1:n.*915T=
NM_001271069.2:c.144+17875T= NP_001257998.1:n.144+17875T=
NM_197957.4:c.171+17875T= NP_932061.1:n.171+17875T=