Canonical Allele Identifier: CA2142951626
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076530C= , CM000676.2:g.65076530C= GRCh38
NC_000014.8:g.65543248C= , CM000676.1:g.65543248C= GRCh37
NC_000014.7:g.64613001C= NCBI36
NG_029830.1:g.30980G= , LRG_530:g.30980G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.210G= ENSP00000452206.2:p.Glu70=
ENST00000556979.6:c.*882G= ENSP00000452378.1:n.*882G=
ENST00000358664.9:c.429G= MANE Select ENSP00000351490.4:p.Glu143=
ENST00000651648.1:c.145-6161G= ENSP00000498863.1:n.145-6161G=
ENST00000284165.10:c.*1273G= ENSP00000284165.6:n.*1273G=
ENST00000341653.6:c.171+17178G= ENSP00000342482.2:n.171+17178G=
ENST00000358402.8:c.402G= ENSP00000351175.4:p.Glu134=
ENST00000358664.8:c.429G= ENSP00000351490.4:p.Glu143=
ENST00000394606.6:c.*202G= ENSP00000378104.2:n.*202G=
ENST00000553928.5:c.*218G= ENSP00000451907.1:n.*218G=
ENST00000555419.5:c.321G= ENSP00000452405.1:p.Glu107=
ENST00000555932.5:c.170G= ENSP00000450763.1:p.Ser57=
ENST00000557277.5:c.240G= ENSP00000450955.1:p.Glu80=
ENST00000618858.4:c.*218G= ENSP00000480127.1:n.*218G=
NM_001271069.1:c.144+17178G= NP_001257998.1:n.144+17178G=
NM_002382.4:c.429G= NP_002373.3:p.Glu143=
NM_145112.2:c.402G= NP_660087.1:p.Glu134=
NM_145113.2:c.*218G= NP_660088.1:n.*218G=
NM_197957.3:c.171+17178G= NP_932061.1:n.171+17178G=
NR_073137.1:n.553G=
XR_429315.2:n.716G=
NM_001320415.1:c.240G= NP_001307344.1:p.Glu80=
XM_017021312.2:c.240G= XP_016876801.1:p.Glu80=
XM_017021313.1:c.240G= XP_016876802.1:p.Glu80=
XR_001750326.2:n.774G=
XR_001750327.2:n.693G=
XR_002957553.1:n.1207G=
XR_943450.3:n.797G=
XR_943451.3:n.813G=
XR_943452.3:n.758G=
NM_001320415.2:c.240G= NP_001307344.1:p.Glu80=
NM_002382.5:c.429G= MANE Select NP_002373.3:p.Glu143=
NM_145112.3:c.402G= NP_660087.1:p.Glu134=
NM_145113.3:c.*218G= NP_660088.1:n.*218G=
NM_001271069.2:c.144+17178G= NP_001257998.1:n.144+17178G=
NM_197957.4:c.171+17178G= NP_932061.1:n.171+17178G=