Canonical Allele Identifier: CA390031267
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076512G>A , CM000676.2:g.65076512G>A GRCh38
NC_000014.8:g.65543230G>A , CM000676.1:g.65543230G>A GRCh37
NC_000014.7:g.64612983G>A NCBI36
NG_029830.1:g.30998C>T , LRG_530:g.30998C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.228C>T ENSP00000452206.2:p.Pro76=
ENST00000556979.6:c.*900C>T ENSP00000452378.1:n.*900C>T
ENST00000358664.9:c.447C>T MANE Select ENSP00000351490.4:p.Pro149=
ENST00000651648.1:c.145-6143C>T ENSP00000498863.1:n.145-6143C>T
ENST00000284165.10:c.*1291C>T ENSP00000284165.6:n.*1291C>T
ENST00000341653.6:c.171+17196C>T ENSP00000342482.2:n.171+17196C>T
ENST00000358402.8:c.420C>T ENSP00000351175.4:p.Pro140=
ENST00000358664.8:c.447C>T ENSP00000351490.4:p.Pro149=
ENST00000394606.6:c.*220C>T ENSP00000378104.2:n.*220C>T
ENST00000553928.5:c.*236C>T ENSP00000451907.1:n.*236C>T
ENST00000555419.5:c.339C>T ENSP00000452405.1:p.Pro113=
ENST00000555932.5:c.188C>T ENSP00000450763.1:p.Pro63Leu
ENST00000557277.5:c.258C>T ENSP00000450955.1:p.Pro86=
ENST00000618858.4:c.*236C>T ENSP00000480127.1:n.*236C>T
NM_001271069.1:c.144+17196C>T NP_001257998.1:n.144+17196C>T
NM_002382.4:c.447C>T NP_002373.3:p.Pro149=
NM_145112.2:c.420C>T NP_660087.1:p.Pro140=
NM_145113.2:c.*236C>T NP_660088.1:n.*236C>T
NM_197957.3:c.171+17196C>T NP_932061.1:n.171+17196C>T
NR_073137.1:n.571C>T
XR_429315.2:n.734C>T
NM_001320415.1:c.258C>T NP_001307344.1:p.Pro86=
XM_017021312.2:c.258C>T XP_016876801.1:p.Pro86=
XM_017021313.1:c.258C>T XP_016876802.1:p.Pro86=
XR_001750326.2:n.792C>T
XR_001750327.2:n.711C>T
XR_002957553.1:n.1225C>T
XR_943450.3:n.815C>T
XR_943451.3:n.831C>T
XR_943452.3:n.776C>T
NM_001320415.2:c.258C>T NP_001307344.1:p.Pro86=
NM_002382.5:c.447C>T MANE Select NP_002373.3:p.Pro149=
NM_145112.3:c.420C>T NP_660087.1:p.Pro140=
NM_145113.3:c.*236C>T NP_660088.1:n.*236C>T
NM_001271069.2:c.144+17196C>T NP_001257998.1:n.144+17196C>T
NM_197957.4:c.171+17196C>T NP_932061.1:n.171+17196C>T