Canonical Allele Identifier: CA2625288876

Gene: MAX

Linked Data

• gnomAD v4: 14-65075322-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075324dup , CM000676.2:g.65075324dup	GRCh38
NC_000014.8:g.65542042dup , CM000676.1:g.65542042dup	GRCh37
NC_000014.7:g.64611795dup	NCBI36
NG_029830.1:g.32187dup , LRG_530:g.32187dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*2089dup	ENSP00000452378.1:n.*2089dup
ENST00000358664.9:c.*1153dup MANE Select	ENSP00000351490.4:n.*1153dup
ENST00000651648.1:c.145-4954dup	ENSP00000498863.1:n.145-4954dup
ENST00000284165.10:c.*2480dup	ENSP00000284165.6:n.*2480dup
ENST00000341653.6:c.171+18385dup	ENSP00000342482.2:n.171+18385dup
ENST00000358402.8:c.*1153dup	ENSP00000351175.4:n.*1153dup
ENST00000394606.6:c.*1409dup	ENSP00000378104.2:n.*1409dup
ENST00000555932.5:c.*1128dup	ENSP00000450763.1:n.*1128dup
ENST00000618858.4:c.*1425dup	ENSP00000480127.1:n.*1425dup
NM_001271069.1:c.144+18385dup	NP_001257998.1:n.144+18385dup
NM_002382.4:c.*1153dup	NP_002373.3:n.*1153dup
NM_145112.2:c.*1153dup	NP_660087.1:n.*1153dup
NM_145113.2:c.*1425dup	NP_660088.1:n.*1425dup
NM_197957.3:c.171+18385dup	NP_932061.1:n.171+18385dup
NR_073137.1:n.1760dup
XR_429315.2:n.1923dup
NM_001320415.1:c.*1153dup	NP_001307344.1:n.*1153dup
XM_017021312.2:c.*1153dup	XP_016876801.1:n.*1153dup
XM_017021313.1:c.*1153dup	XP_016876802.1:n.*1153dup
XR_001750326.2:n.1981dup
XR_001750327.2:n.1900dup
XR_002957553.1:n.2414dup
XR_943450.3:n.2004dup
XR_943451.3:n.2020dup
XR_943452.3:n.1965dup
NM_001320415.2:c.*1153dup	NP_001307344.1:n.*1153dup
NM_002382.5:c.*1153dup MANE Select	NP_002373.3:n.*1153dup
NM_145112.3:c.*1153dup	NP_660087.1:n.*1153dup
NM_145113.3:c.*1425dup	NP_660088.1:n.*1425dup
NM_001271069.2:c.144+18385dup	NP_001257998.1:n.144+18385dup
NM_197957.4:c.171+18385dup	NP_932061.1:n.171+18385dup