Canonical Allele Identifier: CA2142951673
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076623C= , CM000676.2:g.65076623C= GRCh38
NC_000014.8:g.65543341C= , CM000676.1:g.65543341C= GRCh37
NC_000014.7:g.64613094C= NCBI36
NG_029830.1:g.30887G= , LRG_530:g.30887G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.117G= ENSP00000452206.2:p.Gln39=
ENST00000556979.6:c.*789G= ENSP00000452378.1:n.*789G=
ENST00000358664.9:c.336G= MANE Select ENSP00000351490.4:p.Gln112=
ENST00000651648.1:c.145-6254G= ENSP00000498863.1:n.145-6254G=
ENST00000284165.10:c.*1180G= ENSP00000284165.6:n.*1180G=
ENST00000341653.6:c.171+17085G= ENSP00000342482.2:n.171+17085G=
ENST00000358402.8:c.309G= ENSP00000351175.4:p.Gln103=
ENST00000358664.8:c.336G= ENSP00000351490.4:p.Gln112=
ENST00000394606.6:c.*109G= ENSP00000378104.2:n.*109G=
ENST00000553928.5:c.*125G= ENSP00000451907.1:n.*125G=
ENST00000555419.5:c.228G= ENSP00000452405.1:p.Gln76=
ENST00000555932.5:c.77G= ENSP00000450763.1:p.Arg26=
ENST00000556892.5:c.117G= ENSP00000452206.1:p.Gln39=
ENST00000557277.5:c.147G= ENSP00000450955.1:p.Gln49=
ENST00000618858.4:c.*125G= ENSP00000480127.1:n.*125G=
NM_001271069.1:c.144+17085G= NP_001257998.1:n.144+17085G=
NM_002382.4:c.336G= NP_002373.3:p.Gln112=
NM_145112.2:c.309G= NP_660087.1:p.Gln103=
NM_145113.2:c.*125G= NP_660088.1:n.*125G=
NM_197957.3:c.171+17085G= NP_932061.1:n.171+17085G=
NR_073137.1:n.460G=
XR_429315.2:n.623G=
XR_943450.1:n.704G=
XR_943451.1:n.720G=
XR_943452.1:n.666G=
NM_001320415.1:c.147G= NP_001307344.1:p.Gln49=
XM_017021312.2:c.147G= XP_016876801.1:p.Gln49=
XM_017021313.1:c.147G= XP_016876802.1:p.Gln49=
XR_001750326.2:n.681G=
XR_001750327.2:n.600G=
XR_002957553.1:n.1114G=
XR_943450.3:n.704G=
XR_943451.3:n.720G=
XR_943452.3:n.665G=
NM_001320415.2:c.147G= NP_001307344.1:p.Gln49=
NM_002382.5:c.336G= MANE Select NP_002373.3:p.Gln112=
NM_145112.3:c.309G= NP_660087.1:p.Gln103=
NM_145113.3:c.*125G= NP_660088.1:n.*125G=
NM_001271069.2:c.144+17085G= NP_001257998.1:n.144+17085G=
NM_197957.4:c.171+17085G= NP_932061.1:n.171+17085G=