Canonical Allele Identifier: CA2142951572

Gene: MAX

Linked Data

• dbSNP Id: rs2063055338

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076402dup , CM000676.2:g.65076402dup	GRCh38
NC_000014.8:g.65543120dup , CM000676.1:g.65543120dup	GRCh37
NC_000014.7:g.64612873dup	NCBI36
NG_029830.1:g.31108dup , LRG_530:g.31108dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*74dup	ENSP00000452206.2:n.*74dup
ENST00000556979.6:c.*1010dup	ENSP00000452378.1:n.*1010dup
ENST00000358664.9:c.*74dup MANE Select	ENSP00000351490.4:n.*74dup
ENST00000651648.1:c.145-6033dup	ENSP00000498863.1:n.145-6033dup
ENST00000284165.10:c.*1401dup	ENSP00000284165.6:n.*1401dup
ENST00000341653.6:c.171+17306dup	ENSP00000342482.2:n.171+17306dup
ENST00000358402.8:c.*74dup	ENSP00000351175.4:n.*74dup
ENST00000358664.8:c.*74dup	ENSP00000351490.4:n.*74dup
ENST00000394606.6:c.*330dup	ENSP00000378104.2:n.*330dup
ENST00000555419.5:c.449dup	ENSP00000452405.1:n.449dup
ENST00000555932.5:c.*49dup	ENSP00000450763.1:n.*49dup
ENST00000618858.4:c.*346dup	ENSP00000480127.1:n.*346dup
NM_001271069.1:c.144+17306dup	NP_001257998.1:n.144+17306dup
NM_002382.4:c.*74dup	NP_002373.3:n.*74dup
NM_145112.2:c.*74dup	NP_660087.1:n.*74dup
NM_145113.2:c.*346dup	NP_660088.1:n.*346dup
NM_197957.3:c.171+17306dup	NP_932061.1:n.171+17306dup
NR_073137.1:n.681dup
XR_429315.2:n.844dup
NM_001320415.1:c.*74dup	NP_001307344.1:n.*74dup
XM_017021312.2:c.*74dup	XP_016876801.1:n.*74dup
XM_017021313.1:c.*74dup	XP_016876802.1:n.*74dup
XR_001750326.2:n.902dup
XR_001750327.2:n.821dup
XR_002957553.1:n.1335dup
XR_943450.3:n.925dup
XR_943451.3:n.941dup
XR_943452.3:n.886dup
NM_001320415.2:c.*74dup	NP_001307344.1:n.*74dup
NM_002382.5:c.*74dup MANE Select	NP_002373.3:n.*74dup
NM_145112.3:c.*74dup	NP_660087.1:n.*74dup
NM_145113.3:c.*346dup	NP_660088.1:n.*346dup
NM_001271069.2:c.144+17306dup	NP_001257998.1:n.144+17306dup
NM_197957.4:c.171+17306dup	NP_932061.1:n.171+17306dup