Canonical Allele Identifier: CA2625292105
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65102421A>G , CM000676.2:g.65102421A>G GRCh38
NC_000014.8:g.65569139A>G , CM000676.1:g.65569139A>G GRCh37
NC_000014.7:g.64638892A>G NCBI36
NG_029830.1:g.5089T>C , LRG_530:g.5089T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000556892.6:c.-157+88T>C ENSP00000452206.2:n.-157+88T>C
ENST00000556979.6:c.-82T>C ENSP00000452378.1:n.-82T>C
ENST00000358664.9:c.-82T>C MANE Select ENSP00000351490.4:n.-82T>C
ENST00000246163.2:c.-82T>C ENSP00000246163.2:n.-82T>C
ENST00000284165.10:c.-82T>C ENSP00000284165.6:n.-82T>C
ENST00000358402.8:c.-82T>C ENSP00000351175.4:n.-82T>C
ENST00000358664.8:c.-82T>C ENSP00000351490.4:n.-82T>C
ENST00000394606.6:c.-82T>C ENSP00000378104.2:n.-82T>C
ENST00000554709.1:n.97T>C
ENST00000555667.5:c.-82T>C ENSP00000452286.1:n.-82T>C
ENST00000555932.5:c.-82T>C ENSP00000450763.1:n.-82T>C
ENST00000556443.5:c.-82T>C ENSP00000450818.1:n.-82T>C
ENST00000556702.1:n.58T>C
ENST00000556892.5:c.-157+88T>C ENSP00000452206.1:n.-157+88T>C
ENST00000556979.5:c.-82T>C ENSP00000452378.1:n.-82T>C
ENST00000557277.5:c.-239+88T>C ENSP00000450955.1:n.-239+88T>C
ENST00000557746.5:c.-82T>C ENSP00000452197.1:n.-82T>C
ENST00000618858.4:c.-82T>C ENSP00000480127.1:n.-82T>C
NM_001271068.1:c.-82T>C NP_001257997.1:n.-82T>C
NM_001271069.1:c.-82T>C NP_001257998.1:n.-82T>C
NM_002382.4:c.-82T>C NP_002373.3:n.-82T>C
NM_145112.2:c.-82T>C NP_660087.1:n.-82T>C
NM_145113.2:c.-82T>C NP_660088.1:n.-82T>C
NM_145114.2:c.-82T>C NP_660089.1:n.-82T>C
NM_197957.3:c.-82T>C NP_932061.1:n.-82T>C
NR_073137.1:n.187+88T>C
NR_073138.1:n.187+88T>C
XM_011536773.1:c.-82T>C XP_011535075.1:n.-82T>C
XR_429315.2:n.121T>C
XR_943450.1:n.121T>C
XR_943451.1:n.121T>C
XR_943452.1:n.110T>C
NM_001320415.1:c.-356T>C NP_001307344.1:n.-356T>C
XM_011536773.3:c.-82T>C XP_011535075.1:n.-82T>C
XM_017021312.2:c.-329T>C XP_016876801.1:n.-329T>C
XR_001750326.2:n.109T>C
XR_001750327.2:n.109T>C
XR_002957553.1:n.112T>C
XR_943450.3:n.121T>C
XR_943451.3:n.121T>C
XR_943452.3:n.109T>C
NM_001320415.2:c.-356T>C NP_001307344.1:n.-356T>C
NM_002382.5:c.-82T>C MANE Select NP_002373.3:n.-82T>C
NM_145112.3:c.-82T>C NP_660087.1:n.-82T>C
NM_145113.3:c.-82T>C NP_660088.1:n.-82T>C
NM_001271068.2:c.-82T>C NP_001257997.1:n.-82T>C
NM_001271069.2:c.-82T>C NP_001257998.1:n.-82T>C
NM_145114.3:c.-82T>C NP_660089.1:n.-82T>C
NM_197957.4:c.-82T>C NP_932061.1:n.-82T>C