Canonical Allele Identifier: CA2142951643
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076568T= , CM000676.2:g.65076568T= GRCh38
NC_000014.8:g.65543286T= , CM000676.1:g.65543286T= GRCh37
NC_000014.7:g.64613039T= NCBI36
NG_029830.1:g.30942A= , LRG_530:g.30942A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.172A= ENSP00000452206.2:p.Ile58=
ENST00000556979.6:c.*844A= ENSP00000452378.1:n.*844A=
ENST00000358664.9:c.391A= MANE Select ENSP00000351490.4:p.Ile131=
ENST00000651648.1:c.145-6199A= ENSP00000498863.1:n.145-6199A=
ENST00000284165.10:c.*1235A= ENSP00000284165.6:n.*1235A=
ENST00000341653.6:c.171+17140A= ENSP00000342482.2:n.171+17140A=
ENST00000358402.8:c.364A= ENSP00000351175.4:p.Ile122=
ENST00000358664.8:c.391A= ENSP00000351490.4:p.Ile131=
ENST00000394606.6:c.*164A= ENSP00000378104.2:n.*164A=
ENST00000553928.5:c.*180A= ENSP00000451907.1:n.*180A=
ENST00000555419.5:c.283A= ENSP00000452405.1:p.Ile95=
ENST00000555932.5:c.132A= ENSP00000450763.1:p.Pro44=
ENST00000557277.5:c.202A= ENSP00000450955.1:p.Ile68=
ENST00000618858.4:c.*180A= ENSP00000480127.1:n.*180A=
NM_001271069.1:c.144+17140A= NP_001257998.1:n.144+17140A=
NM_002382.4:c.391A= NP_002373.3:p.Ile131=
NM_145112.2:c.364A= NP_660087.1:p.Ile122=
NM_145113.2:c.*180A= NP_660088.1:n.*180A=
NM_197957.3:c.171+17140A= NP_932061.1:n.171+17140A=
NR_073137.1:n.515A=
XR_429315.2:n.678A=
NM_001320415.1:c.202A= NP_001307344.1:p.Ile68=
XM_017021312.2:c.202A= XP_016876801.1:p.Ile68=
XM_017021313.1:c.202A= XP_016876802.1:p.Ile68=
XR_001750326.2:n.736A=
XR_001750327.2:n.655A=
XR_002957553.1:n.1169A=
XR_943450.3:n.759A=
XR_943451.3:n.775A=
XR_943452.3:n.720A=
NM_001320415.2:c.202A= NP_001307344.1:p.Ile68=
NM_002382.5:c.391A= MANE Select NP_002373.3:p.Ile131=
NM_145112.3:c.364A= NP_660087.1:p.Ile122=
NM_145113.3:c.*180A= NP_660088.1:n.*180A=
NM_001271069.2:c.144+17140A= NP_001257998.1:n.144+17140A=
NM_197957.4:c.171+17140A= NP_932061.1:n.171+17140A=