Canonical Allele Identifier: CA2625289764

Gene: MAX

Linked Data

• gnomAD v4: 14-65076400-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076400G>T , CM000676.2:g.65076400G>T	GRCh38
NC_000014.8:g.65543118G>T , CM000676.1:g.65543118G>T	GRCh37
NC_000014.7:g.64612871G>T	NCBI36
NG_029830.1:g.31110C>A , LRG_530:g.31110C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*76C>A	ENSP00000452206.2:n.*76C>A
ENST00000556979.6:c.*1012C>A	ENSP00000452378.1:n.*1012C>A
ENST00000358664.9:c.*76C>A MANE Select	ENSP00000351490.4:n.*76C>A
ENST00000651648.1:c.145-6031C>A	ENSP00000498863.1:n.145-6031C>A
ENST00000284165.10:c.*1403C>A	ENSP00000284165.6:n.*1403C>A
ENST00000341653.6:c.171+17308C>A	ENSP00000342482.2:n.171+17308C>A
ENST00000358402.8:c.*76C>A	ENSP00000351175.4:n.*76C>A
ENST00000358664.8:c.*76C>A	ENSP00000351490.4:n.*76C>A
ENST00000394606.6:c.*332C>A	ENSP00000378104.2:n.*332C>A
ENST00000555419.5:c.451C>A	ENSP00000452405.1:n.451C>A
ENST00000555932.5:c.*51C>A	ENSP00000450763.1:n.*51C>A
ENST00000618858.4:c.*348C>A	ENSP00000480127.1:n.*348C>A
NM_001271069.1:c.144+17308C>A	NP_001257998.1:n.144+17308C>A
NM_002382.4:c.*76C>A	NP_002373.3:n.*76C>A
NM_145112.2:c.*76C>A	NP_660087.1:n.*76C>A
NM_145113.2:c.*348C>A	NP_660088.1:n.*348C>A
NM_197957.3:c.171+17308C>A	NP_932061.1:n.171+17308C>A
NR_073137.1:n.683C>A
XR_429315.2:n.846C>A
NM_001320415.1:c.*76C>A	NP_001307344.1:n.*76C>A
XM_017021312.2:c.*76C>A	XP_016876801.1:n.*76C>A
XM_017021313.1:c.*76C>A	XP_016876802.1:n.*76C>A
XR_001750326.2:n.904C>A
XR_001750327.2:n.823C>A
XR_002957553.1:n.1337C>A
XR_943450.3:n.927C>A
XR_943451.3:n.943C>A
XR_943452.3:n.888C>A
NM_001320415.2:c.*76C>A	NP_001307344.1:n.*76C>A
NM_002382.5:c.*76C>A MANE Select	NP_002373.3:n.*76C>A
NM_145112.3:c.*76C>A	NP_660087.1:n.*76C>A
NM_145113.3:c.*348C>A	NP_660088.1:n.*348C>A
NM_001271069.2:c.144+17308C>A	NP_001257998.1:n.144+17308C>A
NM_197957.4:c.171+17308C>A	NP_932061.1:n.171+17308C>A