Canonical Allele Identifier: CA2625289213

Gene: MAX

Linked Data

• gnomAD v4: 14-65075832-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075832G>T , CM000676.2:g.65075832G>T	GRCh38
NC_000014.8:g.65542550G>T , CM000676.1:g.65542550G>T	GRCh37
NC_000014.7:g.64612303G>T	NCBI36
NG_029830.1:g.31678C>A , LRG_530:g.31678C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000556892.6:c.*644C>A	ENSP00000452206.2:n.*644C>A
ENST00000556979.6:c.*1580C>A	ENSP00000452378.1:n.*1580C>A
ENST00000358664.9:c.*644C>A MANE Select	ENSP00000351490.4:n.*644C>A
ENST00000651648.1:c.145-5463C>A	ENSP00000498863.1:n.145-5463C>A
ENST00000284165.10:c.*1971C>A	ENSP00000284165.6:n.*1971C>A
ENST00000341653.6:c.171+17876C>A	ENSP00000342482.2:n.171+17876C>A
ENST00000358402.8:c.*644C>A	ENSP00000351175.4:n.*644C>A
ENST00000358664.8:c.*644C>A	ENSP00000351490.4:n.*644C>A
ENST00000394606.6:c.*900C>A	ENSP00000378104.2:n.*900C>A
ENST00000555932.5:c.*619C>A	ENSP00000450763.1:n.*619C>A
ENST00000618858.4:c.*916C>A	ENSP00000480127.1:n.*916C>A
NM_001271069.1:c.144+17876C>A	NP_001257998.1:n.144+17876C>A
NM_002382.4:c.*644C>A	NP_002373.3:n.*644C>A
NM_145112.2:c.*644C>A	NP_660087.1:n.*644C>A
NM_145113.2:c.*916C>A	NP_660088.1:n.*916C>A
NM_197957.3:c.171+17876C>A	NP_932061.1:n.171+17876C>A
NR_073137.1:n.1251C>A
XR_429315.2:n.1414C>A
NM_001320415.1:c.*644C>A	NP_001307344.1:n.*644C>A
XM_017021312.2:c.*644C>A	XP_016876801.1:n.*644C>A
XM_017021313.1:c.*644C>A	XP_016876802.1:n.*644C>A
XR_001750326.2:n.1472C>A
XR_001750327.2:n.1391C>A
XR_002957553.1:n.1905C>A
XR_943450.3:n.1495C>A
XR_943451.3:n.1511C>A
XR_943452.3:n.1456C>A
NM_001320415.2:c.*644C>A	NP_001307344.1:n.*644C>A
NM_002382.5:c.*644C>A MANE Select	NP_002373.3:n.*644C>A
NM_145112.3:c.*644C>A	NP_660087.1:n.*644C>A
NM_145113.3:c.*916C>A	NP_660088.1:n.*916C>A
NM_001271069.2:c.144+17876C>A	NP_001257998.1:n.144+17876C>A
NM_197957.4:c.171+17876C>A	NP_932061.1:n.171+17876C>A