Canonical Allele Identifier: CA2142951583
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076424G= , CM000676.2:g.65076424G= GRCh38
NC_000014.8:g.65543142G= , CM000676.1:g.65543142G= GRCh37
NC_000014.7:g.64612895G= NCBI36
NG_029830.1:g.31086C= , LRG_530:g.31086C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*52C= ENSP00000452206.2:n.*52C=
ENST00000556979.6:c.*988C= ENSP00000452378.1:n.*988C=
ENST00000358664.9:c.*52C= MANE Select ENSP00000351490.4:n.*52C=
ENST00000651648.1:c.145-6055C= ENSP00000498863.1:n.145-6055C=
ENST00000284165.10:c.*1379C= ENSP00000284165.6:n.*1379C=
ENST00000341653.6:c.171+17284C= ENSP00000342482.2:n.171+17284C=
ENST00000358402.8:c.*52C= ENSP00000351175.4:n.*52C=
ENST00000358664.8:c.*52C= ENSP00000351490.4:n.*52C=
ENST00000394606.6:c.*308C= ENSP00000378104.2:n.*308C=
ENST00000555419.5:c.427C= ENSP00000452405.1:n.427C=
ENST00000555932.5:c.*27C= ENSP00000450763.1:n.*27C=
ENST00000618858.4:c.*324C= ENSP00000480127.1:n.*324C=
NM_001271069.1:c.144+17284C= NP_001257998.1:n.144+17284C=
NM_002382.4:c.*52C= NP_002373.3:n.*52C=
NM_145112.2:c.*52C= NP_660087.1:n.*52C=
NM_145113.2:c.*324C= NP_660088.1:n.*324C=
NM_197957.3:c.171+17284C= NP_932061.1:n.171+17284C=
NR_073137.1:n.659C=
XR_429315.2:n.822C=
NM_001320415.1:c.*52C= NP_001307344.1:n.*52C=
XM_017021312.2:c.*52C= XP_016876801.1:n.*52C=
XM_017021313.1:c.*52C= XP_016876802.1:n.*52C=
XR_001750326.2:n.880C=
XR_001750327.2:n.799C=
XR_002957553.1:n.1313C=
XR_943450.3:n.903C=
XR_943451.3:n.919C=
XR_943452.3:n.864C=
NM_001320415.2:c.*52C= NP_001307344.1:n.*52C=
NM_002382.5:c.*52C= MANE Select NP_002373.3:n.*52C=
NM_145112.3:c.*52C= NP_660087.1:n.*52C=
NM_145113.3:c.*324C= NP_660088.1:n.*324C=
NM_001271069.2:c.144+17284C= NP_001257998.1:n.144+17284C=
NM_197957.4:c.171+17284C= NP_932061.1:n.171+17284C=