Canonical Allele Identifier: CA2142951652
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076585T= , CM000676.2:g.65076585T= GRCh38
NC_000014.8:g.65543303T= , CM000676.1:g.65543303T= GRCh37
NC_000014.7:g.64613056T= NCBI36
NG_029830.1:g.30925A= , LRG_530:g.30925A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.155A= ENSP00000452206.2:p.Asn52=
ENST00000556979.6:c.*827A= ENSP00000452378.1:n.*827A=
ENST00000358664.9:c.374A= MANE Select ENSP00000351490.4:p.Asn125=
ENST00000651648.1:c.145-6216A= ENSP00000498863.1:n.145-6216A=
ENST00000284165.10:c.*1218A= ENSP00000284165.6:n.*1218A=
ENST00000341653.6:c.171+17123A= ENSP00000342482.2:n.171+17123A=
ENST00000358402.8:c.347A= ENSP00000351175.4:p.Asn116=
ENST00000358664.8:c.374A= ENSP00000351490.4:p.Asn125=
ENST00000394606.6:c.*147A= ENSP00000378104.2:n.*147A=
ENST00000553928.5:c.*163A= ENSP00000451907.1:n.*163A=
ENST00000555419.5:c.266A= ENSP00000452405.1:p.Asn89=
ENST00000555932.5:c.115A= ENSP00000450763.1:p.Thr39=
ENST00000557277.5:c.185A= ENSP00000450955.1:p.Asn62=
ENST00000618858.4:c.*163A= ENSP00000480127.1:n.*163A=
NM_001271069.1:c.144+17123A= NP_001257998.1:n.144+17123A=
NM_002382.4:c.374A= NP_002373.3:p.Asn125=
NM_145112.2:c.347A= NP_660087.1:p.Asn116=
NM_145113.2:c.*163A= NP_660088.1:n.*163A=
NM_197957.3:c.171+17123A= NP_932061.1:n.171+17123A=
NR_073137.1:n.498A=
XR_429315.2:n.661A=
XR_943450.1:n.742A=
XR_943451.1:n.758A=
XR_943452.1:n.704A=
NM_001320415.1:c.185A= NP_001307344.1:p.Asn62=
XM_017021312.2:c.185A= XP_016876801.1:p.Asn62=
XM_017021313.1:c.185A= XP_016876802.1:p.Asn62=
XR_001750326.2:n.719A=
XR_001750327.2:n.638A=
XR_002957553.1:n.1152A=
XR_943450.3:n.742A=
XR_943451.3:n.758A=
XR_943452.3:n.703A=
NM_001320415.2:c.185A= NP_001307344.1:p.Asn62=
NM_002382.5:c.374A= MANE Select NP_002373.3:p.Asn125=
NM_145112.3:c.347A= NP_660087.1:p.Asn116=
NM_145113.3:c.*163A= NP_660088.1:n.*163A=
NM_001271069.2:c.144+17123A= NP_001257998.1:n.144+17123A=
NM_197957.4:c.171+17123A= NP_932061.1:n.171+17123A=