Canonical Allele Identifier: CA2625289216

Gene: MAX

Linked Data

• gnomAD v4: 14-65075838-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075838A>C , CM000676.2:g.65075838A>C	GRCh38
NC_000014.8:g.65542556A>C , CM000676.1:g.65542556A>C	GRCh37
NC_000014.7:g.64612309A>C	NCBI36
NG_029830.1:g.31672T>G , LRG_530:g.31672T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000556892.6:c.*638T>G	ENSP00000452206.2:n.*638T>G
ENST00000556979.6:c.*1574T>G	ENSP00000452378.1:n.*1574T>G
ENST00000358664.9:c.*638T>G MANE Select	ENSP00000351490.4:n.*638T>G
ENST00000651648.1:c.145-5469T>G	ENSP00000498863.1:n.145-5469T>G
ENST00000284165.10:c.*1965T>G	ENSP00000284165.6:n.*1965T>G
ENST00000341653.6:c.171+17870T>G	ENSP00000342482.2:n.171+17870T>G
ENST00000358402.8:c.*638T>G	ENSP00000351175.4:n.*638T>G
ENST00000358664.8:c.*638T>G	ENSP00000351490.4:n.*638T>G
ENST00000394606.6:c.*894T>G	ENSP00000378104.2:n.*894T>G
ENST00000555932.5:c.*613T>G	ENSP00000450763.1:n.*613T>G
ENST00000618858.4:c.*910T>G	ENSP00000480127.1:n.*910T>G
NM_001271069.1:c.144+17870T>G	NP_001257998.1:n.144+17870T>G
NM_002382.4:c.*638T>G	NP_002373.3:n.*638T>G
NM_145112.2:c.*638T>G	NP_660087.1:n.*638T>G
NM_145113.2:c.*910T>G	NP_660088.1:n.*910T>G
NM_197957.3:c.171+17870T>G	NP_932061.1:n.171+17870T>G
NR_073137.1:n.1245T>G
XR_429315.2:n.1408T>G
NM_001320415.1:c.*638T>G	NP_001307344.1:n.*638T>G
XM_017021312.2:c.*638T>G	XP_016876801.1:n.*638T>G
XM_017021313.1:c.*638T>G	XP_016876802.1:n.*638T>G
XR_001750326.2:n.1466T>G
XR_001750327.2:n.1385T>G
XR_002957553.1:n.1899T>G
XR_943450.3:n.1489T>G
XR_943451.3:n.1505T>G
XR_943452.3:n.1450T>G
NM_001320415.2:c.*638T>G	NP_001307344.1:n.*638T>G
NM_002382.5:c.*638T>G MANE Select	NP_002373.3:n.*638T>G
NM_145112.3:c.*638T>G	NP_660087.1:n.*638T>G
NM_145113.3:c.*910T>G	NP_660088.1:n.*910T>G
NM_001271069.2:c.144+17870T>G	NP_001257998.1:n.144+17870T>G
NM_197957.4:c.171+17870T>G	NP_932061.1:n.171+17870T>G