Canonical Allele Identifier: CA2142952270
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65078011T= , CM000676.2:g.65078011T= GRCh38
NC_000014.8:g.65544729T= , CM000676.1:g.65544729T= GRCh37
NC_000014.7:g.64614482T= NCBI36
NG_029830.1:g.29499A= , LRG_530:g.29499A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.-23A= ENSP00000452206.2:n.-23A=
ENST00000556979.6:c.197A= ENSP00000452378.1:p.Lys66=
ENST00000358664.9:c.197A= MANE Select ENSP00000351490.4:p.Lys66=
ENST00000651648.1:c.145-7642A= ENSP00000498863.1:n.145-7642A=
ENST00000284165.10:c.197A= ENSP00000284165.6:p.Lys66=
ENST00000341653.6:c.171+15697A= ENSP00000342482.2:n.171+15697A=
ENST00000358402.8:c.170A= ENSP00000351175.4:p.Lys57=
ENST00000358664.8:c.197A= ENSP00000351490.4:p.Lys66=
ENST00000394606.6:c.197A= ENSP00000378104.2:p.Lys66=
ENST00000553928.5:c.197A= ENSP00000451907.1:p.Lys66=
ENST00000553951.1:n.274A=
ENST00000555419.5:c.89A= ENSP00000452405.1:p.Lys30=
ENST00000555667.5:c.170A= ENSP00000452286.1:p.Lys57=
ENST00000555932.5:c.37-1348A= ENSP00000450763.1:n.37-1348A=
ENST00000556443.5:c.170A= ENSP00000450818.1:p.Lys57=
ENST00000556892.5:c.-23A= ENSP00000452206.1:n.-23A=
ENST00000556979.5:c.197A= ENSP00000452378.1:p.Lys66=
ENST00000557277.5:c.-78A= ENSP00000450955.1:n.-78A=
ENST00000557746.5:c.170A= ENSP00000452197.1:p.Lys57=
ENST00000618858.4:c.197A= ENSP00000480127.1:p.Lys66=
NM_001271069.1:c.144+15697A= NP_001257998.1:n.144+15697A=
NM_002382.4:c.197A= NP_002373.3:p.Lys66=
NM_145112.2:c.170A= NP_660087.1:p.Lys57=
NM_145113.2:c.197A= NP_660088.1:p.Lys66=
NM_197957.3:c.171+15697A= NP_932061.1:n.171+15697A=
NR_073137.1:n.321A=
XM_011536773.1:c.197A= XP_011535075.1:p.Lys66=
XR_429315.2:n.399A=
XR_943450.1:n.399A=
XR_943451.1:n.399A=
XR_943452.1:n.361A=
NM_001320415.1:c.-78A= NP_001307344.1:n.-78A=
XM_011536773.3:c.197A= XP_011535075.1:p.Lys66=
XM_017021312.2:c.-78A= XP_016876801.1:n.-78A=
XM_017021313.1:c.-78A= XP_016876802.1:n.-78A=
XR_001750326.2:n.360A=
XR_001750327.2:n.360A=
XR_002957553.1:n.390A=
XR_943450.3:n.399A=
XR_943451.3:n.399A=
XR_943452.3:n.360A=
NM_001320415.2:c.-78A= NP_001307344.1:n.-78A=
NM_002382.5:c.197A= MANE Select NP_002373.3:p.Lys66=
NM_145112.3:c.170A= NP_660087.1:p.Lys57=
NM_145113.3:c.197A= NP_660088.1:p.Lys66=
NM_001271069.2:c.144+15697A= NP_001257998.1:n.144+15697A=
NM_197957.4:c.171+15697A= NP_932061.1:n.171+15697A=