Canonical Allele Identifier: CA2625289436

Gene: MAX

Linked Data

• gnomAD v4: 14-65076039-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076039T>C , CM000676.2:g.65076039T>C	GRCh38
NC_000014.8:g.65542757T>C , CM000676.1:g.65542757T>C	GRCh37
NC_000014.7:g.64612510T>C	NCBI36
NG_029830.1:g.31471A>G , LRG_530:g.31471A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*437A>G	ENSP00000452206.2:n.*437A>G
ENST00000556979.6:c.*1373A>G	ENSP00000452378.1:n.*1373A>G
ENST00000358664.9:c.*437A>G MANE Select	ENSP00000351490.4:n.*437A>G
ENST00000651648.1:c.145-5670A>G	ENSP00000498863.1:n.145-5670A>G
ENST00000284165.10:c.*1764A>G	ENSP00000284165.6:n.*1764A>G
ENST00000341653.6:c.171+17669A>G	ENSP00000342482.2:n.171+17669A>G
ENST00000358402.8:c.*437A>G	ENSP00000351175.4:n.*437A>G
ENST00000358664.8:c.*437A>G	ENSP00000351490.4:n.*437A>G
ENST00000394606.6:c.*693A>G	ENSP00000378104.2:n.*693A>G
ENST00000555932.5:c.*412A>G	ENSP00000450763.1:n.*412A>G
ENST00000618858.4:c.*709A>G	ENSP00000480127.1:n.*709A>G
NM_001271069.1:c.144+17669A>G	NP_001257998.1:n.144+17669A>G
NM_002382.4:c.*437A>G	NP_002373.3:n.*437A>G
NM_145112.2:c.*437A>G	NP_660087.1:n.*437A>G
NM_145113.2:c.*709A>G	NP_660088.1:n.*709A>G
NM_197957.3:c.171+17669A>G	NP_932061.1:n.171+17669A>G
NR_073137.1:n.1044A>G
XR_429315.2:n.1207A>G
NM_001320415.1:c.*437A>G	NP_001307344.1:n.*437A>G
XM_017021312.2:c.*437A>G	XP_016876801.1:n.*437A>G
XM_017021313.1:c.*437A>G	XP_016876802.1:n.*437A>G
XR_001750326.2:n.1265A>G
XR_001750327.2:n.1184A>G
XR_002957553.1:n.1698A>G
XR_943450.3:n.1288A>G
XR_943451.3:n.1304A>G
XR_943452.3:n.1249A>G
NM_001320415.2:c.*437A>G	NP_001307344.1:n.*437A>G
NM_002382.5:c.*437A>G MANE Select	NP_002373.3:n.*437A>G
NM_145112.3:c.*437A>G	NP_660087.1:n.*437A>G
NM_145113.3:c.*709A>G	NP_660088.1:n.*709A>G
NM_001271069.2:c.144+17669A>G	NP_001257998.1:n.144+17669A>G
NM_197957.4:c.171+17669A>G	NP_932061.1:n.171+17669A>G