Canonical Allele Identifier: CA2142951653
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076586T= , CM000676.2:g.65076586T= GRCh38
NC_000014.8:g.65543304T= , CM000676.1:g.65543304T= GRCh37
NC_000014.7:g.64613057T= NCBI36
NG_029830.1:g.30924A= , LRG_530:g.30924A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.154A= ENSP00000452206.2:p.Asn52=
ENST00000556979.6:c.*826A= ENSP00000452378.1:n.*826A=
ENST00000358664.9:c.373A= MANE Select ENSP00000351490.4:p.Asn125=
ENST00000651648.1:c.145-6217A= ENSP00000498863.1:n.145-6217A=
ENST00000284165.10:c.*1217A= ENSP00000284165.6:n.*1217A=
ENST00000341653.6:c.171+17122A= ENSP00000342482.2:n.171+17122A=
ENST00000358402.8:c.346A= ENSP00000351175.4:p.Asn116=
ENST00000358664.8:c.373A= ENSP00000351490.4:p.Asn125=
ENST00000394606.6:c.*146A= ENSP00000378104.2:n.*146A=
ENST00000553928.5:c.*162A= ENSP00000451907.1:n.*162A=
ENST00000555419.5:c.265A= ENSP00000452405.1:p.Asn89=
ENST00000555932.5:c.114A= ENSP00000450763.1:p.Pro38=
ENST00000557277.5:c.184A= ENSP00000450955.1:p.Asn62=
ENST00000618858.4:c.*162A= ENSP00000480127.1:n.*162A=
NM_001271069.1:c.144+17122A= NP_001257998.1:n.144+17122A=
NM_002382.4:c.373A= NP_002373.3:p.Asn125=
NM_145112.2:c.346A= NP_660087.1:p.Asn116=
NM_145113.2:c.*162A= NP_660088.1:n.*162A=
NM_197957.3:c.171+17122A= NP_932061.1:n.171+17122A=
NR_073137.1:n.497A=
XR_429315.2:n.660A=
XR_943450.1:n.741A=
XR_943451.1:n.757A=
XR_943452.1:n.703A=
NM_001320415.1:c.184A= NP_001307344.1:p.Asn62=
XM_017021312.2:c.184A= XP_016876801.1:p.Asn62=
XM_017021313.1:c.184A= XP_016876802.1:p.Asn62=
XR_001750326.2:n.718A=
XR_001750327.2:n.637A=
XR_002957553.1:n.1151A=
XR_943450.3:n.741A=
XR_943451.3:n.757A=
XR_943452.3:n.702A=
NM_001320415.2:c.184A= NP_001307344.1:p.Asn62=
NM_002382.5:c.373A= MANE Select NP_002373.3:p.Asn125=
NM_145112.3:c.346A= NP_660087.1:p.Asn116=
NM_145113.3:c.*162A= NP_660088.1:n.*162A=
NM_001271069.2:c.144+17122A= NP_001257998.1:n.144+17122A=
NM_197957.4:c.171+17122A= NP_932061.1:n.171+17122A=