Canonical Allele Identifier: CA2142951636
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076551C= , CM000676.2:g.65076551C= GRCh38
NC_000014.8:g.65543269C= , CM000676.1:g.65543269C= GRCh37
NC_000014.7:g.64613022C= NCBI36
NG_029830.1:g.30959G= , LRG_530:g.30959G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.189G= ENSP00000452206.2:p.Gly63=
ENST00000556979.6:c.*861G= ENSP00000452378.1:n.*861G=
ENST00000358664.9:c.408G= MANE Select ENSP00000351490.4:p.Gly136=
ENST00000651648.1:c.145-6182G= ENSP00000498863.1:n.145-6182G=
ENST00000284165.10:c.*1252G= ENSP00000284165.6:n.*1252G=
ENST00000341653.6:c.171+17157G= ENSP00000342482.2:n.171+17157G=
ENST00000358402.8:c.381G= ENSP00000351175.4:p.Gly127=
ENST00000358664.8:c.408G= ENSP00000351490.4:p.Gly136=
ENST00000394606.6:c.*181G= ENSP00000378104.2:n.*181G=
ENST00000553928.5:c.*197G= ENSP00000451907.1:n.*197G=
ENST00000555419.5:c.300G= ENSP00000452405.1:p.Gly100=
ENST00000555932.5:c.149G= ENSP00000450763.1:p.Gly50=
ENST00000557277.5:c.219G= ENSP00000450955.1:p.Gly73=
ENST00000618858.4:c.*197G= ENSP00000480127.1:n.*197G=
NM_001271069.1:c.144+17157G= NP_001257998.1:n.144+17157G=
NM_002382.4:c.408G= NP_002373.3:p.Gly136=
NM_145112.2:c.381G= NP_660087.1:p.Gly127=
NM_145113.2:c.*197G= NP_660088.1:n.*197G=
NM_197957.3:c.171+17157G= NP_932061.1:n.171+17157G=
NR_073137.1:n.532G=
XR_429315.2:n.695G=
NM_001320415.1:c.219G= NP_001307344.1:p.Gly73=
XM_017021312.2:c.219G= XP_016876801.1:p.Gly73=
XM_017021313.1:c.219G= XP_016876802.1:p.Gly73=
XR_001750326.2:n.753G=
XR_001750327.2:n.672G=
XR_002957553.1:n.1186G=
XR_943450.3:n.776G=
XR_943451.3:n.792G=
XR_943452.3:n.737G=
NM_001320415.2:c.219G= NP_001307344.1:p.Gly73=
NM_002382.5:c.408G= MANE Select NP_002373.3:p.Gly136=
NM_145112.3:c.381G= NP_660087.1:p.Gly127=
NM_145113.3:c.*197G= NP_660088.1:n.*197G=
NM_001271069.2:c.144+17157G= NP_001257998.1:n.144+17157G=
NM_197957.4:c.171+17157G= NP_932061.1:n.171+17157G=