Canonical Allele Identifier: CA2142951215
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075671C= , CM000676.2:g.65075671C= GRCh38
NC_000014.8:g.65542389C= , CM000676.1:g.65542389C= GRCh37
NC_000014.7:g.64612142C= NCBI36
NG_029830.1:g.31839G= , LRG_530:g.31839G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*805G= ENSP00000452206.2:n.*805G=
ENST00000556979.6:c.*1741G= ENSP00000452378.1:n.*1741G=
ENST00000358664.9:c.*805G= MANE Select ENSP00000351490.4:n.*805G=
ENST00000651648.1:c.145-5302G= ENSP00000498863.1:n.145-5302G=
ENST00000284165.10:c.*2132G= ENSP00000284165.6:n.*2132G=
ENST00000341653.6:c.171+18037G= ENSP00000342482.2:n.171+18037G=
ENST00000358402.8:c.*805G= ENSP00000351175.4:n.*805G=
ENST00000358664.8:c.*805G= ENSP00000351490.4:n.*805G=
ENST00000394606.6:c.*1061G= ENSP00000378104.2:n.*1061G=
ENST00000555932.5:c.*780G= ENSP00000450763.1:n.*780G=
ENST00000618858.4:c.*1077G= ENSP00000480127.1:n.*1077G=
NM_001271069.1:c.144+18037G= NP_001257998.1:n.144+18037G=
NM_002382.4:c.*805G= NP_002373.3:n.*805G=
NM_145112.2:c.*805G= NP_660087.1:n.*805G=
NM_145113.2:c.*1077G= NP_660088.1:n.*1077G=
NM_197957.3:c.171+18037G= NP_932061.1:n.171+18037G=
NR_073137.1:n.1412G=
XR_429315.2:n.1575G=
NM_001320415.1:c.*805G= NP_001307344.1:n.*805G=
XM_017021312.2:c.*805G= XP_016876801.1:n.*805G=
XM_017021313.1:c.*805G= XP_016876802.1:n.*805G=
XR_001750326.2:n.1633G=
XR_001750327.2:n.1552G=
XR_002957553.1:n.2066G=
XR_943450.3:n.1656G=
XR_943451.3:n.1672G=
XR_943452.3:n.1617G=
NM_001320415.2:c.*805G= NP_001307344.1:n.*805G=
NM_002382.5:c.*805G= MANE Select NP_002373.3:n.*805G=
NM_145112.3:c.*805G= NP_660087.1:n.*805G=
NM_145113.3:c.*1077G= NP_660088.1:n.*1077G=
NM_001271069.2:c.144+18037G= NP_001257998.1:n.144+18037G=
NM_197957.4:c.171+18037G= NP_932061.1:n.171+18037G=