Canonical Allele Identifier: CA2142951638
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076554A= , CM000676.2:g.65076554A= GRCh38
NC_000014.8:g.65543272A= , CM000676.1:g.65543272A= GRCh37
NC_000014.7:g.64613025A= NCBI36
NG_029830.1:g.30956T= , LRG_530:g.30956T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.186T= ENSP00000452206.2:p.Asp62=
ENST00000556979.6:c.*858T= ENSP00000452378.1:n.*858T=
ENST00000358664.9:c.405T= MANE Select ENSP00000351490.4:p.Asp135=
ENST00000651648.1:c.145-6185T= ENSP00000498863.1:n.145-6185T=
ENST00000284165.10:c.*1249T= ENSP00000284165.6:n.*1249T=
ENST00000341653.6:c.171+17154T= ENSP00000342482.2:n.171+17154T=
ENST00000358402.8:c.378T= ENSP00000351175.4:p.Asp126=
ENST00000358664.8:c.405T= ENSP00000351490.4:p.Asp135=
ENST00000394606.6:c.*178T= ENSP00000378104.2:n.*178T=
ENST00000553928.5:c.*194T= ENSP00000451907.1:n.*194T=
ENST00000555419.5:c.297T= ENSP00000452405.1:p.Asp99=
ENST00000555932.5:c.146T= ENSP00000450763.1:p.Met49=
ENST00000557277.5:c.216T= ENSP00000450955.1:p.Asp72=
ENST00000618858.4:c.*194T= ENSP00000480127.1:n.*194T=
NM_001271069.1:c.144+17154T= NP_001257998.1:n.144+17154T=
NM_002382.4:c.405T= NP_002373.3:p.Asp135=
NM_145112.2:c.378T= NP_660087.1:p.Asp126=
NM_145113.2:c.*194T= NP_660088.1:n.*194T=
NM_197957.3:c.171+17154T= NP_932061.1:n.171+17154T=
NR_073137.1:n.529T=
XR_429315.2:n.692T=
NM_001320415.1:c.216T= NP_001307344.1:p.Asp72=
XM_017021312.2:c.216T= XP_016876801.1:p.Asp72=
XM_017021313.1:c.216T= XP_016876802.1:p.Asp72=
XR_001750326.2:n.750T=
XR_001750327.2:n.669T=
XR_002957553.1:n.1183T=
XR_943450.3:n.773T=
XR_943451.3:n.789T=
XR_943452.3:n.734T=
NM_001320415.2:c.216T= NP_001307344.1:p.Asp72=
NM_002382.5:c.405T= MANE Select NP_002373.3:p.Asp135=
NM_145112.3:c.378T= NP_660087.1:p.Asp126=
NM_145113.3:c.*194T= NP_660088.1:n.*194T=
NM_001271069.2:c.144+17154T= NP_001257998.1:n.144+17154T=
NM_197957.4:c.171+17154T= NP_932061.1:n.171+17154T=