Canonical Allele Identifier: CA2625289542

Gene: MAX

Linked Data

• gnomAD v4: 14-65076104-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076104C>T , CM000676.2:g.65076104C>T	GRCh38
NC_000014.8:g.65542822C>T , CM000676.1:g.65542822C>T	GRCh37
NC_000014.7:g.64612575C>T	NCBI36
NG_029830.1:g.31406G>A , LRG_530:g.31406G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*372G>A	ENSP00000452206.2:n.*372G>A
ENST00000556979.6:c.*1308G>A	ENSP00000452378.1:n.*1308G>A
ENST00000358664.9:c.*372G>A MANE Select	ENSP00000351490.4:n.*372G>A
ENST00000651648.1:c.145-5735G>A	ENSP00000498863.1:n.145-5735G>A
ENST00000284165.10:c.*1699G>A	ENSP00000284165.6:n.*1699G>A
ENST00000341653.6:c.171+17604G>A	ENSP00000342482.2:n.171+17604G>A
ENST00000358402.8:c.*372G>A	ENSP00000351175.4:n.*372G>A
ENST00000358664.8:c.*372G>A	ENSP00000351490.4:n.*372G>A
ENST00000394606.6:c.*628G>A	ENSP00000378104.2:n.*628G>A
ENST00000555419.5:c.747G>A	ENSP00000452405.1:n.747G>A
ENST00000555932.5:c.*347G>A	ENSP00000450763.1:n.*347G>A
ENST00000618858.4:c.*644G>A	ENSP00000480127.1:n.*644G>A
NM_001271069.1:c.144+17604G>A	NP_001257998.1:n.144+17604G>A
NM_002382.4:c.*372G>A	NP_002373.3:n.*372G>A
NM_145112.2:c.*372G>A	NP_660087.1:n.*372G>A
NM_145113.2:c.*644G>A	NP_660088.1:n.*644G>A
NM_197957.3:c.171+17604G>A	NP_932061.1:n.171+17604G>A
NR_073137.1:n.979G>A
XR_429315.2:n.1142G>A
NM_001320415.1:c.*372G>A	NP_001307344.1:n.*372G>A
XM_017021312.2:c.*372G>A	XP_016876801.1:n.*372G>A
XM_017021313.1:c.*372G>A	XP_016876802.1:n.*372G>A
XR_001750326.2:n.1200G>A
XR_001750327.2:n.1119G>A
XR_002957553.1:n.1633G>A
XR_943450.3:n.1223G>A
XR_943451.3:n.1239G>A
XR_943452.3:n.1184G>A
NM_001320415.2:c.*372G>A	NP_001307344.1:n.*372G>A
NM_002382.5:c.*372G>A MANE Select	NP_002373.3:n.*372G>A
NM_145112.3:c.*372G>A	NP_660087.1:n.*372G>A
NM_145113.3:c.*644G>A	NP_660088.1:n.*644G>A
NM_001271069.2:c.144+17604G>A	NP_001257998.1:n.144+17604G>A
NM_197957.4:c.171+17604G>A	NP_932061.1:n.171+17604G>A