Canonical Allele Identifier: CA2801909146

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65102221dup , CM000676.2:g.65102221dup	GRCh38
NC_000014.8:g.65568939dup , CM000676.1:g.65568939dup	GRCh37
NC_000014.7:g.64638692dup	NCBI36
NG_029830.1:g.5293dup , LRG_530:g.5293dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.-157+292dup	ENSP00000452206.2:n.-157+292dup
ENST00000556979.6:c.36+87dup	ENSP00000452378.1:n.36+87dup
ENST00000358664.9:c.36+87dup MANE Select	ENSP00000351490.4:n.36+87dup
ENST00000651648.1:c.36+87dup	ENSP00000498863.1:n.36+87dup
ENST00000246163.2:c.36+87dup	ENSP00000246163.2:n.36+87dup
ENST00000284165.10:c.36+87dup	ENSP00000284165.6:n.36+87dup
ENST00000341653.6:c.36+87dup	ENSP00000342482.2:n.36+87dup
ENST00000358402.8:c.36+87dup	ENSP00000351175.4:n.36+87dup
ENST00000358664.8:c.36+87dup	ENSP00000351490.4:n.36+87dup
ENST00000394606.6:c.36+87dup	ENSP00000378104.2:n.36+87dup
ENST00000553928.5:c.36+87dup	ENSP00000451907.1:n.36+87dup
ENST00000554709.1:n.214+87dup
ENST00000555419.5:c.36+87dup	ENSP00000452405.1:n.36+87dup
ENST00000555667.5:c.36+87dup	ENSP00000452286.1:n.36+87dup
ENST00000555932.5:c.36+87dup	ENSP00000450763.1:n.36+87dup
ENST00000556443.5:c.36+87dup	ENSP00000450818.1:n.36+87dup
ENST00000556702.1:n.175+87dup
ENST00000556892.5:c.-157+292dup	ENSP00000452206.1:n.-157+292dup
ENST00000556979.5:c.36+87dup	ENSP00000452378.1:n.36+87dup
ENST00000557277.5:c.-239+292dup	ENSP00000450955.1:n.-239+292dup
ENST00000557746.5:c.36+87dup	ENSP00000452197.1:n.36+87dup
ENST00000618858.4:c.36+87dup	ENSP00000480127.1:n.36+87dup
NM_001271068.1:c.36+87dup	NP_001257997.1:n.36+87dup
NM_001271069.1:c.36+87dup	NP_001257998.1:n.36+87dup
NM_002382.4:c.36+87dup	NP_002373.3:n.36+87dup
NM_145112.2:c.36+87dup	NP_660087.1:n.36+87dup
NM_145113.2:c.36+87dup	NP_660088.1:n.36+87dup
NM_145114.2:c.36+87dup	NP_660089.1:n.36+87dup
NM_197957.3:c.36+87dup	NP_932061.1:n.36+87dup
NR_073137.1:n.187+292dup
NR_073138.1:n.187+292dup
XM_011536773.1:c.36+87dup	XP_011535075.1:n.36+87dup
XR_429315.2:n.238+87dup
XR_943450.1:n.238+87dup
XR_943451.1:n.238+87dup
XR_943452.1:n.227+87dup
NM_001320415.1:c.-239+87dup	NP_001307344.1:n.-239+87dup
XM_011536773.3:c.36+87dup	XP_011535075.1:n.36+87dup
XM_017021312.2:c.-212+87dup	XP_016876801.1:n.-212+87dup
XM_017021313.1:c.-350dup	XP_016876802.1:n.-350dup
XR_001750326.2:n.226+87dup
XR_001750327.2:n.226+87dup
XR_002957553.1:n.229+87dup
XR_943450.3:n.238+87dup
XR_943451.3:n.238+87dup
XR_943452.3:n.226+87dup
NM_001320415.2:c.-239+87dup	NP_001307344.1:n.-239+87dup
NM_002382.5:c.36+87dup MANE Select	NP_002373.3:n.36+87dup
NM_145112.3:c.36+87dup	NP_660087.1:n.36+87dup
NM_145113.3:c.36+87dup	NP_660088.1:n.36+87dup
NM_001271068.2:c.36+87dup	NP_001257997.1:n.36+87dup
NM_001271069.2:c.36+87dup	NP_001257998.1:n.36+87dup
NM_145114.3:c.36+87dup	NP_660089.1:n.36+87dup
NM_197957.4:c.36+87dup	NP_932061.1:n.36+87dup