Canonical Allele Identifier: CA2142951587
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076436G= , CM000676.2:g.65076436G= GRCh38
NC_000014.8:g.65543154G= , CM000676.1:g.65543154G= GRCh37
NC_000014.7:g.64612907G= NCBI36
NG_029830.1:g.31074C= , LRG_530:g.31074C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*40C= ENSP00000452206.2:n.*40C=
ENST00000556979.6:c.*976C= ENSP00000452378.1:n.*976C=
ENST00000358664.9:c.*40C= MANE Select ENSP00000351490.4:n.*40C=
ENST00000651648.1:c.145-6067C= ENSP00000498863.1:n.145-6067C=
ENST00000284165.10:c.*1367C= ENSP00000284165.6:n.*1367C=
ENST00000341653.6:c.171+17272C= ENSP00000342482.2:n.171+17272C=
ENST00000358402.8:c.*40C= ENSP00000351175.4:n.*40C=
ENST00000358664.8:c.*40C= ENSP00000351490.4:n.*40C=
ENST00000394606.6:c.*296C= ENSP00000378104.2:n.*296C=
ENST00000555419.5:c.415C= ENSP00000452405.1:n.415C=
ENST00000555932.5:c.*15C= ENSP00000450763.1:n.*15C=
ENST00000618858.4:c.*312C= ENSP00000480127.1:n.*312C=
NM_001271069.1:c.144+17272C= NP_001257998.1:n.144+17272C=
NM_002382.4:c.*40C= NP_002373.3:n.*40C=
NM_145112.2:c.*40C= NP_660087.1:n.*40C=
NM_145113.2:c.*312C= NP_660088.1:n.*312C=
NM_197957.3:c.171+17272C= NP_932061.1:n.171+17272C=
NR_073137.1:n.647C=
XR_429315.2:n.810C=
NM_001320415.1:c.*40C= NP_001307344.1:n.*40C=
XM_017021312.2:c.*40C= XP_016876801.1:n.*40C=
XM_017021313.1:c.*40C= XP_016876802.1:n.*40C=
XR_001750326.2:n.868C=
XR_001750327.2:n.787C=
XR_002957553.1:n.1301C=
XR_943450.3:n.891C=
XR_943451.3:n.907C=
XR_943452.3:n.852C=
NM_001320415.2:c.*40C= NP_001307344.1:n.*40C=
NM_002382.5:c.*40C= MANE Select NP_002373.3:n.*40C=
NM_145112.3:c.*40C= NP_660087.1:n.*40C=
NM_145113.3:c.*312C= NP_660088.1:n.*312C=
NM_001271069.2:c.144+17272C= NP_001257998.1:n.144+17272C=
NM_197957.4:c.171+17272C= NP_932061.1:n.171+17272C=