Canonical Allele Identifier: CA2801908497

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075704dup , CM000676.2:g.65075704dup	GRCh38
NC_000014.8:g.65542422dup , CM000676.1:g.65542422dup	GRCh37
NC_000014.7:g.64612175dup	NCBI36
NG_029830.1:g.31806dup , LRG_530:g.31806dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*772dup	ENSP00000452206.2:n.*772dup
ENST00000556979.6:c.*1708dup	ENSP00000452378.1:n.*1708dup
ENST00000358664.9:c.*772dup MANE Select	ENSP00000351490.4:n.*772dup
ENST00000651648.1:c.145-5335dup	ENSP00000498863.1:n.145-5335dup
ENST00000284165.10:c.*2099dup	ENSP00000284165.6:n.*2099dup
ENST00000341653.6:c.171+18004dup	ENSP00000342482.2:n.171+18004dup
ENST00000358402.8:c.*772dup	ENSP00000351175.4:n.*772dup
ENST00000358664.8:c.*772dup	ENSP00000351490.4:n.*772dup
ENST00000394606.6:c.*1028dup	ENSP00000378104.2:n.*1028dup
ENST00000555932.5:c.*747dup	ENSP00000450763.1:n.*747dup
ENST00000618858.4:c.*1044dup	ENSP00000480127.1:n.*1044dup
NM_001271069.1:c.144+18004dup	NP_001257998.1:n.144+18004dup
NM_002382.4:c.*772dup	NP_002373.3:n.*772dup
NM_145112.2:c.*772dup	NP_660087.1:n.*772dup
NM_145113.2:c.*1044dup	NP_660088.1:n.*1044dup
NM_197957.3:c.171+18004dup	NP_932061.1:n.171+18004dup
NR_073137.1:n.1379dup
XR_429315.2:n.1542dup
NM_001320415.1:c.*772dup	NP_001307344.1:n.*772dup
XM_017021312.2:c.*772dup	XP_016876801.1:n.*772dup
XM_017021313.1:c.*772dup	XP_016876802.1:n.*772dup
XR_001750326.2:n.1600dup
XR_001750327.2:n.1519dup
XR_002957553.1:n.2033dup
XR_943450.3:n.1623dup
XR_943451.3:n.1639dup
XR_943452.3:n.1584dup
NM_001320415.2:c.*772dup	NP_001307344.1:n.*772dup
NM_002382.5:c.*772dup MANE Select	NP_002373.3:n.*772dup
NM_145112.3:c.*772dup	NP_660087.1:n.*772dup
NM_145113.3:c.*1044dup	NP_660088.1:n.*1044dup
NM_001271069.2:c.144+18004dup	NP_001257998.1:n.144+18004dup
NM_197957.4:c.171+18004dup	NP_932061.1:n.171+18004dup