Canonical Allele Identifier: CA2142951086
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075376G= , CM000676.2:g.65075376G= GRCh38
NC_000014.8:g.65542094G= , CM000676.1:g.65542094G= GRCh37
NC_000014.7:g.64611847G= NCBI36
NG_029830.1:g.32134C= , LRG_530:g.32134C=

Transcript Alleles

HGVS Amino-acid change
ENST00000556979.6:c.*2036C= ENSP00000452378.1:n.*2036C=
ENST00000358664.9:c.*1100C= MANE Select ENSP00000351490.4:n.*1100C=
ENST00000651648.1:c.145-5007C= ENSP00000498863.1:n.145-5007C=
ENST00000284165.10:c.*2427C= ENSP00000284165.6:n.*2427C=
ENST00000341653.6:c.171+18332C= ENSP00000342482.2:n.171+18332C=
ENST00000358402.8:c.*1100C= ENSP00000351175.4:n.*1100C=
ENST00000394606.6:c.*1356C= ENSP00000378104.2:n.*1356C=
ENST00000555932.5:c.*1075C= ENSP00000450763.1:n.*1075C=
ENST00000618858.4:c.*1372C= ENSP00000480127.1:n.*1372C=
NM_001271069.1:c.144+18332C= NP_001257998.1:n.144+18332C=
NM_002382.4:c.*1100C= NP_002373.3:n.*1100C=
NM_145112.2:c.*1100C= NP_660087.1:n.*1100C=
NM_145113.2:c.*1372C= NP_660088.1:n.*1372C=
NM_197957.3:c.171+18332C= NP_932061.1:n.171+18332C=
NR_073137.1:n.1707C=
XR_429315.2:n.1870C=
NM_001320415.1:c.*1100C= NP_001307344.1:n.*1100C=
XM_017021312.2:c.*1100C= XP_016876801.1:n.*1100C=
XM_017021313.1:c.*1100C= XP_016876802.1:n.*1100C=
XR_001750326.2:n.1928C=
XR_001750327.2:n.1847C=
XR_002957553.1:n.2361C=
XR_943450.3:n.1951C=
XR_943451.3:n.1967C=
XR_943452.3:n.1912C=
NM_001320415.2:c.*1100C= NP_001307344.1:n.*1100C=
NM_002382.5:c.*1100C= MANE Select NP_002373.3:n.*1100C=
NM_145112.3:c.*1100C= NP_660087.1:n.*1100C=
NM_145113.3:c.*1372C= NP_660088.1:n.*1372C=
NM_001271069.2:c.144+18332C= NP_001257998.1:n.144+18332C=
NM_197957.4:c.171+18332C= NP_932061.1:n.171+18332C=