Canonical Allele Identifier: CA390031843
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076618T>A , CM000676.2:g.65076618T>A GRCh38
NC_000014.8:g.65543336T>A , CM000676.1:g.65543336T>A GRCh37
NC_000014.7:g.64613089T>A NCBI36
NG_029830.1:g.30892A>T , LRG_530:g.30892A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.122A>T ENSP00000452206.2:p.Asn41Ile
ENST00000556979.6:c.*794A>T ENSP00000452378.1:n.*794A>T
ENST00000358664.9:c.341A>T MANE Select ENSP00000351490.4:p.Asn114Ile
ENST00000651648.1:c.145-6249A>T ENSP00000498863.1:n.145-6249A>T
ENST00000284165.10:c.*1185A>T ENSP00000284165.6:n.*1185A>T
ENST00000341653.6:c.171+17090A>T ENSP00000342482.2:n.171+17090A>T
ENST00000358402.8:c.314A>T ENSP00000351175.4:p.Asn105Ile
ENST00000358664.8:c.341A>T ENSP00000351490.4:p.Asn114Ile
ENST00000394606.6:c.*114A>T ENSP00000378104.2:n.*114A>T
ENST00000553928.5:c.*130A>T ENSP00000451907.1:n.*130A>T
ENST00000555419.5:c.233A>T ENSP00000452405.1:p.Asn78Ile
ENST00000555932.5:c.82A>T ENSP00000450763.1:p.Thr28Ser
ENST00000556892.5:c.122A>T ENSP00000452206.1:p.Asn41Ile
ENST00000557277.5:c.152A>T ENSP00000450955.1:p.Asn51Ile
ENST00000618858.4:c.*130A>T ENSP00000480127.1:n.*130A>T
NM_001271069.1:c.144+17090A>T NP_001257998.1:n.144+17090A>T
NM_002382.4:c.341A>T NP_002373.3:p.Asn114Ile
NM_145112.2:c.314A>T NP_660087.1:p.Asn105Ile
NM_145113.2:c.*130A>T NP_660088.1:n.*130A>T
NM_197957.3:c.171+17090A>T NP_932061.1:n.171+17090A>T
NR_073137.1:n.465A>T
XR_429315.2:n.628A>T
XR_943450.1:n.709A>T
XR_943451.1:n.725A>T
XR_943452.1:n.671A>T
NM_001320415.1:c.152A>T NP_001307344.1:p.Asn51Ile
XM_017021312.2:c.152A>T XP_016876801.1:p.Asn51Ile
XM_017021313.1:c.152A>T XP_016876802.1:p.Asn51Ile
XR_001750326.2:n.686A>T
XR_001750327.2:n.605A>T
XR_002957553.1:n.1119A>T
XR_943450.3:n.709A>T
XR_943451.3:n.725A>T
XR_943452.3:n.670A>T
NM_001320415.2:c.152A>T NP_001307344.1:p.Asn51Ile
NM_002382.5:c.341A>T MANE Select NP_002373.3:p.Asn114Ile
NM_145112.3:c.314A>T NP_660087.1:p.Asn105Ile
NM_145113.3:c.*130A>T NP_660088.1:n.*130A>T
NM_001271069.2:c.144+17090A>T NP_001257998.1:n.144+17090A>T
NM_197957.4:c.171+17090A>T NP_932061.1:n.171+17090A>T