Canonical Allele Identifier: CA2142951642
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076566G= , CM000676.2:g.65076566G= GRCh38
NC_000014.8:g.65543284G= , CM000676.1:g.65543284G= GRCh37
NC_000014.7:g.64613037G= NCBI36
NG_029830.1:g.30944C= , LRG_530:g.30944C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.174C= ENSP00000452206.2:p.Ile58=
ENST00000556979.6:c.*846C= ENSP00000452378.1:n.*846C=
ENST00000358664.9:c.393C= MANE Select ENSP00000351490.4:p.Ile131=
ENST00000651648.1:c.145-6197C= ENSP00000498863.1:n.145-6197C=
ENST00000284165.10:c.*1237C= ENSP00000284165.6:n.*1237C=
ENST00000341653.6:c.171+17142C= ENSP00000342482.2:n.171+17142C=
ENST00000358402.8:c.366C= ENSP00000351175.4:p.Ile122=
ENST00000358664.8:c.393C= ENSP00000351490.4:p.Ile131=
ENST00000394606.6:c.*166C= ENSP00000378104.2:n.*166C=
ENST00000553928.5:c.*182C= ENSP00000451907.1:n.*182C=
ENST00000555419.5:c.285C= ENSP00000452405.1:p.Ile95=
ENST00000555932.5:c.134C= ENSP00000450763.1:p.Ser45=
ENST00000557277.5:c.204C= ENSP00000450955.1:p.Ile68=
ENST00000618858.4:c.*182C= ENSP00000480127.1:n.*182C=
NM_001271069.1:c.144+17142C= NP_001257998.1:n.144+17142C=
NM_002382.4:c.393C= NP_002373.3:p.Ile131=
NM_145112.2:c.366C= NP_660087.1:p.Ile122=
NM_145113.2:c.*182C= NP_660088.1:n.*182C=
NM_197957.3:c.171+17142C= NP_932061.1:n.171+17142C=
NR_073137.1:n.517C=
XR_429315.2:n.680C=
NM_001320415.1:c.204C= NP_001307344.1:p.Ile68=
XM_017021312.2:c.204C= XP_016876801.1:p.Ile68=
XM_017021313.1:c.204C= XP_016876802.1:p.Ile68=
XR_001750326.2:n.738C=
XR_001750327.2:n.657C=
XR_002957553.1:n.1171C=
XR_943450.3:n.761C=
XR_943451.3:n.777C=
XR_943452.3:n.722C=
NM_001320415.2:c.204C= NP_001307344.1:p.Ile68=
NM_002382.5:c.393C= MANE Select NP_002373.3:p.Ile131=
NM_145112.3:c.366C= NP_660087.1:p.Ile122=
NM_145113.3:c.*182C= NP_660088.1:n.*182C=
NM_001271069.2:c.144+17142C= NP_001257998.1:n.144+17142C=
NM_197957.4:c.171+17142C= NP_932061.1:n.171+17142C=