Canonical Allele Identifier: CA2142951324
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075879G= , CM000676.2:g.65075879G= GRCh38
NC_000014.8:g.65542597G= , CM000676.1:g.65542597G= GRCh37
NC_000014.7:g.64612350G= NCBI36
NG_029830.1:g.31631C= , LRG_530:g.31631C=

Transcript Alleles

HGVS Amino-acid change
ENST00000556892.6:c.*597C= ENSP00000452206.2:n.*597C=
ENST00000556979.6:c.*1533C= ENSP00000452378.1:n.*1533C=
ENST00000358664.9:c.*597C= MANE Select ENSP00000351490.4:n.*597C=
ENST00000651648.1:c.145-5510C= ENSP00000498863.1:n.145-5510C=
ENST00000284165.10:c.*1924C= ENSP00000284165.6:n.*1924C=
ENST00000341653.6:c.171+17829C= ENSP00000342482.2:n.171+17829C=
ENST00000358402.8:c.*597C= ENSP00000351175.4:n.*597C=
ENST00000358664.8:c.*597C= ENSP00000351490.4:n.*597C=
ENST00000394606.6:c.*853C= ENSP00000378104.2:n.*853C=
ENST00000555932.5:c.*572C= ENSP00000450763.1:n.*572C=
ENST00000618858.4:c.*869C= ENSP00000480127.1:n.*869C=
NM_001271069.1:c.144+17829C= NP_001257998.1:n.144+17829C=
NM_002382.4:c.*597C= NP_002373.3:n.*597C=
NM_145112.2:c.*597C= NP_660087.1:n.*597C=
NM_145113.2:c.*869C= NP_660088.1:n.*869C=
NM_197957.3:c.171+17829C= NP_932061.1:n.171+17829C=
NR_073137.1:n.1204C=
XR_429315.2:n.1367C=
NM_001320415.1:c.*597C= NP_001307344.1:n.*597C=
XM_017021312.2:c.*597C= XP_016876801.1:n.*597C=
XM_017021313.1:c.*597C= XP_016876802.1:n.*597C=
XR_001750326.2:n.1425C=
XR_001750327.2:n.1344C=
XR_002957553.1:n.1858C=
XR_943450.3:n.1448C=
XR_943451.3:n.1464C=
XR_943452.3:n.1409C=
NM_001320415.2:c.*597C= NP_001307344.1:n.*597C=
NM_002382.5:c.*597C= MANE Select NP_002373.3:n.*597C=
NM_145112.3:c.*597C= NP_660087.1:n.*597C=
NM_145113.3:c.*869C= NP_660088.1:n.*869C=
NM_001271069.2:c.144+17829C= NP_001257998.1:n.144+17829C=
NM_197957.4:c.171+17829C= NP_932061.1:n.171+17829C=