Canonical Allele Identifier: CA2142951012
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075214T= , CM000676.2:g.65075214T= GRCh38
NC_000014.8:g.65541932T= , CM000676.1:g.65541932T= GRCh37
NC_000014.7:g.64611685T= NCBI36
NG_029830.1:g.32296A= , LRG_530:g.32296A=

Transcript Alleles

HGVS Amino-acid change
ENST00000556979.6:c.*2198A= ENSP00000452378.1:n.*2198A=
ENST00000358664.9:c.*1262A= MANE Select ENSP00000351490.4:n.*1262A=
ENST00000651648.1:c.145-4845A= ENSP00000498863.1:n.145-4845A=
ENST00000284165.10:c.*2589A= ENSP00000284165.6:n.*2589A=
ENST00000341653.6:c.171+18494A= ENSP00000342482.2:n.171+18494A=
ENST00000358402.8:c.*1262A= ENSP00000351175.4:n.*1262A=
ENST00000394606.6:c.*1518A= ENSP00000378104.2:n.*1518A=
ENST00000555932.5:c.*1237A= ENSP00000450763.1:n.*1237A=
ENST00000618858.4:c.*1534A= ENSP00000480127.1:n.*1534A=
NM_001271069.1:c.144+18494A= NP_001257998.1:n.144+18494A=
NM_002382.4:c.*1262A= NP_002373.3:n.*1262A=
NM_145112.2:c.*1262A= NP_660087.1:n.*1262A=
NM_145113.2:c.*1534A= NP_660088.1:n.*1534A=
NM_197957.3:c.171+18494A= NP_932061.1:n.171+18494A=
NR_073137.1:n.1869A=
XR_429315.2:n.2032A=
NM_001320415.1:c.*1262A= NP_001307344.1:n.*1262A=
XM_017021312.2:c.*1262A= XP_016876801.1:n.*1262A=
XM_017021313.1:c.*1262A= XP_016876802.1:n.*1262A=
XR_001750326.2:n.2090A=
XR_001750327.2:n.2009A=
XR_002957553.1:n.2523A=
XR_943450.3:n.2113A=
XR_943451.3:n.2129A=
XR_943452.3:n.2074A=
NM_001320415.2:c.*1262A= NP_001307344.1:n.*1262A=
NM_002382.5:c.*1262A= MANE Select NP_002373.3:n.*1262A=
NM_145112.3:c.*1262A= NP_660087.1:n.*1262A=
NM_145113.3:c.*1534A= NP_660088.1:n.*1534A=
NM_001271069.2:c.144+18494A= NP_001257998.1:n.144+18494A=
NM_197957.4:c.171+18494A= NP_932061.1:n.171+18494A=