Canonical Allele Identifier: CA2142951616
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076514G= , CM000676.2:g.65076514G= GRCh38
NC_000014.8:g.65543232G= , CM000676.1:g.65543232G= GRCh37
NC_000014.7:g.64612985G= NCBI36
NG_029830.1:g.30996C= , LRG_530:g.30996C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.226C= ENSP00000452206.2:p.Pro76=
ENST00000556979.6:c.*898C= ENSP00000452378.1:n.*898C=
ENST00000358664.9:c.445C= MANE Select ENSP00000351490.4:p.Pro149=
ENST00000651648.1:c.145-6145C= ENSP00000498863.1:n.145-6145C=
ENST00000284165.10:c.*1289C= ENSP00000284165.6:n.*1289C=
ENST00000341653.6:c.171+17194C= ENSP00000342482.2:n.171+17194C=
ENST00000358402.8:c.418C= ENSP00000351175.4:p.Pro140=
ENST00000358664.8:c.445C= ENSP00000351490.4:p.Pro149=
ENST00000394606.6:c.*218C= ENSP00000378104.2:n.*218C=
ENST00000553928.5:c.*234C= ENSP00000451907.1:n.*234C=
ENST00000555419.5:c.337C= ENSP00000452405.1:p.Pro113=
ENST00000555932.5:c.186C= ENSP00000450763.1:p.Ser62=
ENST00000557277.5:c.256C= ENSP00000450955.1:p.Pro86=
ENST00000618858.4:c.*234C= ENSP00000480127.1:n.*234C=
NM_001271069.1:c.144+17194C= NP_001257998.1:n.144+17194C=
NM_002382.4:c.445C= NP_002373.3:p.Pro149=
NM_145112.2:c.418C= NP_660087.1:p.Pro140=
NM_145113.2:c.*234C= NP_660088.1:n.*234C=
NM_197957.3:c.171+17194C= NP_932061.1:n.171+17194C=
NR_073137.1:n.569C=
XR_429315.2:n.732C=
NM_001320415.1:c.256C= NP_001307344.1:p.Pro86=
XM_017021312.2:c.256C= XP_016876801.1:p.Pro86=
XM_017021313.1:c.256C= XP_016876802.1:p.Pro86=
XR_001750326.2:n.790C=
XR_001750327.2:n.709C=
XR_002957553.1:n.1223C=
XR_943450.3:n.813C=
XR_943451.3:n.829C=
XR_943452.3:n.774C=
NM_001320415.2:c.256C= NP_001307344.1:p.Pro86=
NM_002382.5:c.445C= MANE Select NP_002373.3:p.Pro149=
NM_145112.3:c.418C= NP_660087.1:p.Pro140=
NM_145113.3:c.*234C= NP_660088.1:n.*234C=
NM_001271069.2:c.144+17194C= NP_001257998.1:n.144+17194C=
NM_197957.4:c.171+17194C= NP_932061.1:n.171+17194C=