Canonical Allele Identifier: CA390031429
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076539G>A , CM000676.2:g.65076539G>A GRCh38
NC_000014.8:g.65543257G>A , CM000676.1:g.65543257G>A GRCh37
NC_000014.7:g.64613010G>A NCBI36
NG_029830.1:g.30971C>T , LRG_530:g.30971C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.201C>T ENSP00000452206.2:p.Ser67=
ENST00000556979.6:c.*873C>T ENSP00000452378.1:n.*873C>T
ENST00000358664.9:c.420C>T MANE Select ENSP00000351490.4:p.Ser140=
ENST00000651648.1:c.145-6170C>T ENSP00000498863.1:n.145-6170C>T
ENST00000284165.10:c.*1264C>T ENSP00000284165.6:n.*1264C>T
ENST00000341653.6:c.171+17169C>T ENSP00000342482.2:n.171+17169C>T
ENST00000358402.8:c.393C>T ENSP00000351175.4:p.Ser131=
ENST00000358664.8:c.420C>T ENSP00000351490.4:p.Ser140=
ENST00000394606.6:c.*193C>T ENSP00000378104.2:n.*193C>T
ENST00000553928.5:c.*209C>T ENSP00000451907.1:n.*209C>T
ENST00000555419.5:c.312C>T ENSP00000452405.1:p.Ser104=
ENST00000555932.5:c.161C>T ENSP00000450763.1:p.Pro54Leu
ENST00000557277.5:c.231C>T ENSP00000450955.1:p.Ser77=
ENST00000618858.4:c.*209C>T ENSP00000480127.1:n.*209C>T
NM_001271069.1:c.144+17169C>T NP_001257998.1:n.144+17169C>T
NM_002382.4:c.420C>T NP_002373.3:p.Ser140=
NM_145112.2:c.393C>T NP_660087.1:p.Ser131=
NM_145113.2:c.*209C>T NP_660088.1:n.*209C>T
NM_197957.3:c.171+17169C>T NP_932061.1:n.171+17169C>T
NR_073137.1:n.544C>T
XR_429315.2:n.707C>T
NM_001320415.1:c.231C>T NP_001307344.1:p.Ser77=
XM_017021312.2:c.231C>T XP_016876801.1:p.Ser77=
XM_017021313.1:c.231C>T XP_016876802.1:p.Ser77=
XR_001750326.2:n.765C>T
XR_001750327.2:n.684C>T
XR_002957553.1:n.1198C>T
XR_943450.3:n.788C>T
XR_943451.3:n.804C>T
XR_943452.3:n.749C>T
NM_001320415.2:c.231C>T NP_001307344.1:p.Ser77=
NM_002382.5:c.420C>T MANE Select NP_002373.3:p.Ser140=
NM_145112.3:c.393C>T NP_660087.1:p.Ser131=
NM_145113.3:c.*209C>T NP_660088.1:n.*209C>T
NM_001271069.2:c.144+17169C>T NP_001257998.1:n.144+17169C>T
NM_197957.4:c.171+17169C>T NP_932061.1:n.171+17169C>T