Canonical Allele Identifier: CA390031736
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076584G>C , CM000676.2:g.65076584G>C GRCh38
NC_000014.8:g.65543302G>C , CM000676.1:g.65543302G>C GRCh37
NC_000014.7:g.64613055G>C NCBI36
NG_029830.1:g.30926C>G , LRG_530:g.30926C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.156C>G ENSP00000452206.2:p.Asn52Lys
ENST00000556979.6:c.*828C>G ENSP00000452378.1:n.*828C>G
ENST00000358664.9:c.375C>G MANE Select ENSP00000351490.4:p.Asn125Lys
ENST00000651648.1:c.145-6215C>G ENSP00000498863.1:n.145-6215C>G
ENST00000284165.10:c.*1219C>G ENSP00000284165.6:n.*1219C>G
ENST00000341653.6:c.171+17124C>G ENSP00000342482.2:n.171+17124C>G
ENST00000358402.8:c.348C>G ENSP00000351175.4:p.Asn116Lys
ENST00000358664.8:c.375C>G ENSP00000351490.4:p.Asn125Lys
ENST00000394606.6:c.*148C>G ENSP00000378104.2:n.*148C>G
ENST00000553928.5:c.*164C>G ENSP00000451907.1:n.*164C>G
ENST00000555419.5:c.267C>G ENSP00000452405.1:p.Asn89Lys
ENST00000555932.5:c.116C>G ENSP00000450763.1:p.Thr39Arg
ENST00000557277.5:c.186C>G ENSP00000450955.1:p.Asn62Lys
ENST00000618858.4:c.*164C>G ENSP00000480127.1:n.*164C>G
NM_001271069.1:c.144+17124C>G NP_001257998.1:n.144+17124C>G
NM_002382.4:c.375C>G NP_002373.3:p.Asn125Lys
NM_145112.2:c.348C>G NP_660087.1:p.Asn116Lys
NM_145113.2:c.*164C>G NP_660088.1:n.*164C>G
NM_197957.3:c.171+17124C>G NP_932061.1:n.171+17124C>G
NR_073137.1:n.499C>G
XR_429315.2:n.662C>G
XR_943450.1:n.743C>G
XR_943451.1:n.759C>G
XR_943452.1:n.705C>G
NM_001320415.1:c.186C>G NP_001307344.1:p.Asn62Lys
XM_017021312.2:c.186C>G XP_016876801.1:p.Asn62Lys
XM_017021313.1:c.186C>G XP_016876802.1:p.Asn62Lys
XR_001750326.2:n.720C>G
XR_001750327.2:n.639C>G
XR_002957553.1:n.1153C>G
XR_943450.3:n.743C>G
XR_943451.3:n.759C>G
XR_943452.3:n.704C>G
NM_001320415.2:c.186C>G NP_001307344.1:p.Asn62Lys
NM_002382.5:c.375C>G MANE Select NP_002373.3:p.Asn125Lys
NM_145112.3:c.348C>G NP_660087.1:p.Asn116Lys
NM_145113.3:c.*164C>G NP_660088.1:n.*164C>G
NM_001271069.2:c.144+17124C>G NP_001257998.1:n.144+17124C>G
NM_197957.4:c.171+17124C>G NP_932061.1:n.171+17124C>G