Canonical Allele Identifier: CA2575554411

Gene: MAX

Linked Data

• gnomAD v4: 14-65076014-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076016dup , CM000676.2:g.65076016dup	GRCh38
NC_000014.8:g.65542734dup , CM000676.1:g.65542734dup	GRCh37
NC_000014.7:g.64612487dup	NCBI36
NG_029830.1:g.31495dup , LRG_530:g.31495dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*461dup	ENSP00000452206.2:n.*461dup
ENST00000556979.6:c.*1397dup	ENSP00000452378.1:n.*1397dup
ENST00000358664.9:c.*461dup MANE Select	ENSP00000351490.4:n.*461dup
ENST00000651648.1:c.145-5646dup	ENSP00000498863.1:n.145-5646dup
ENST00000284165.10:c.*1788dup	ENSP00000284165.6:n.*1788dup
ENST00000341653.6:c.171+17693dup	ENSP00000342482.2:n.171+17693dup
ENST00000358402.8:c.*461dup	ENSP00000351175.4:n.*461dup
ENST00000358664.8:c.*461dup	ENSP00000351490.4:n.*461dup
ENST00000394606.6:c.*717dup	ENSP00000378104.2:n.*717dup
ENST00000555932.5:c.*436dup	ENSP00000450763.1:n.*436dup
ENST00000618858.4:c.*733dup	ENSP00000480127.1:n.*733dup
NM_001271069.1:c.144+17693dup	NP_001257998.1:n.144+17693dup
NM_002382.4:c.*461dup	NP_002373.3:n.*461dup
NM_145112.2:c.*461dup	NP_660087.1:n.*461dup
NM_145113.2:c.*733dup	NP_660088.1:n.*733dup
NM_197957.3:c.171+17693dup	NP_932061.1:n.171+17693dup
NR_073137.1:n.1068dup
XR_429315.2:n.1231dup
NM_001320415.1:c.*461dup	NP_001307344.1:n.*461dup
XM_017021312.2:c.*461dup	XP_016876801.1:n.*461dup
XM_017021313.1:c.*461dup	XP_016876802.1:n.*461dup
XR_001750326.2:n.1289dup
XR_001750327.2:n.1208dup
XR_002957553.1:n.1722dup
XR_943450.3:n.1312dup
XR_943451.3:n.1328dup
XR_943452.3:n.1273dup
NM_001320415.2:c.*461dup	NP_001307344.1:n.*461dup
NM_002382.5:c.*461dup MANE Select	NP_002373.3:n.*461dup
NM_145112.3:c.*461dup	NP_660087.1:n.*461dup
NM_145113.3:c.*733dup	NP_660088.1:n.*733dup
NM_001271069.2:c.144+17693dup	NP_001257998.1:n.144+17693dup
NM_197957.4:c.171+17693dup	NP_932061.1:n.171+17693dup