Canonical Allele Identifier: CA2625288954

Gene: MAX

Linked Data

• gnomAD v4: 14-65075419-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075419G>A , CM000676.2:g.65075419G>A	GRCh38
NC_000014.8:g.65542137G>A , CM000676.1:g.65542137G>A	GRCh37
NC_000014.7:g.64611890G>A	NCBI36
NG_029830.1:g.32091C>T , LRG_530:g.32091C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*1993C>T	ENSP00000452378.1:n.*1993C>T
ENST00000358664.9:c.*1057C>T MANE Select	ENSP00000351490.4:n.*1057C>T
ENST00000651648.1:c.145-5050C>T	ENSP00000498863.1:n.145-5050C>T
ENST00000284165.10:c.*2384C>T	ENSP00000284165.6:n.*2384C>T
ENST00000341653.6:c.171+18289C>T	ENSP00000342482.2:n.171+18289C>T
ENST00000358402.8:c.*1057C>T	ENSP00000351175.4:n.*1057C>T
ENST00000394606.6:c.*1313C>T	ENSP00000378104.2:n.*1313C>T
ENST00000555932.5:c.*1032C>T	ENSP00000450763.1:n.*1032C>T
ENST00000618858.4:c.*1329C>T	ENSP00000480127.1:n.*1329C>T
NM_001271069.1:c.144+18289C>T	NP_001257998.1:n.144+18289C>T
NM_002382.4:c.*1057C>T	NP_002373.3:n.*1057C>T
NM_145112.2:c.*1057C>T	NP_660087.1:n.*1057C>T
NM_145113.2:c.*1329C>T	NP_660088.1:n.*1329C>T
NM_197957.3:c.171+18289C>T	NP_932061.1:n.171+18289C>T
NR_073137.1:n.1664C>T
XR_429315.2:n.1827C>T
NM_001320415.1:c.*1057C>T	NP_001307344.1:n.*1057C>T
XM_017021312.2:c.*1057C>T	XP_016876801.1:n.*1057C>T
XM_017021313.1:c.*1057C>T	XP_016876802.1:n.*1057C>T
XR_001750326.2:n.1885C>T
XR_001750327.2:n.1804C>T
XR_002957553.1:n.2318C>T
XR_943450.3:n.1908C>T
XR_943451.3:n.1924C>T
XR_943452.3:n.1869C>T
NM_001320415.2:c.*1057C>T	NP_001307344.1:n.*1057C>T
NM_002382.5:c.*1057C>T MANE Select	NP_002373.3:n.*1057C>T
NM_145112.3:c.*1057C>T	NP_660087.1:n.*1057C>T
NM_145113.3:c.*1329C>T	NP_660088.1:n.*1329C>T
NM_001271069.2:c.144+18289C>T	NP_001257998.1:n.144+18289C>T
NM_197957.4:c.171+18289C>T	NP_932061.1:n.171+18289C>T