Canonical Allele Identifier: CA2142951218
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075676C= , CM000676.2:g.65075676C= GRCh38
NC_000014.8:g.65542394C= , CM000676.1:g.65542394C= GRCh37
NC_000014.7:g.64612147C= NCBI36
NG_029830.1:g.31834G= , LRG_530:g.31834G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*800G= ENSP00000452206.2:n.*800G=
ENST00000556979.6:c.*1736G= ENSP00000452378.1:n.*1736G=
ENST00000358664.9:c.*800G= MANE Select ENSP00000351490.4:n.*800G=
ENST00000651648.1:c.145-5307G= ENSP00000498863.1:n.145-5307G=
ENST00000284165.10:c.*2127G= ENSP00000284165.6:n.*2127G=
ENST00000341653.6:c.171+18032G= ENSP00000342482.2:n.171+18032G=
ENST00000358402.8:c.*800G= ENSP00000351175.4:n.*800G=
ENST00000358664.8:c.*800G= ENSP00000351490.4:n.*800G=
ENST00000394606.6:c.*1056G= ENSP00000378104.2:n.*1056G=
ENST00000555932.5:c.*775G= ENSP00000450763.1:n.*775G=
ENST00000618858.4:c.*1072G= ENSP00000480127.1:n.*1072G=
NM_001271069.1:c.144+18032G= NP_001257998.1:n.144+18032G=
NM_002382.4:c.*800G= NP_002373.3:n.*800G=
NM_145112.2:c.*800G= NP_660087.1:n.*800G=
NM_145113.2:c.*1072G= NP_660088.1:n.*1072G=
NM_197957.3:c.171+18032G= NP_932061.1:n.171+18032G=
NR_073137.1:n.1407G=
XR_429315.2:n.1570G=
NM_001320415.1:c.*800G= NP_001307344.1:n.*800G=
XM_017021312.2:c.*800G= XP_016876801.1:n.*800G=
XM_017021313.1:c.*800G= XP_016876802.1:n.*800G=
XR_001750326.2:n.1628G=
XR_001750327.2:n.1547G=
XR_002957553.1:n.2061G=
XR_943450.3:n.1651G=
XR_943451.3:n.1667G=
XR_943452.3:n.1612G=
NM_001320415.2:c.*800G= NP_001307344.1:n.*800G=
NM_002382.5:c.*800G= MANE Select NP_002373.3:n.*800G=
NM_145112.3:c.*800G= NP_660087.1:n.*800G=
NM_145113.3:c.*1072G= NP_660088.1:n.*1072G=
NM_001271069.2:c.144+18032G= NP_001257998.1:n.144+18032G=
NM_197957.4:c.171+18032G= NP_932061.1:n.171+18032G=