Canonical Allele Identifier: CA707762091

Gene: MAX

Linked Data

• dbSNP Id: rs1333930817
• gnomAD v4: 14-65102431-T-TCC
• MyVariant Identifiers: chr14:g.65569149_65569150insCC (hg19) ; chr14:g.65102431_65102432insCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65102437_65102438dup , CM000676.2:g.65102437_65102438dup	GRCh38
NC_000014.8:g.65569155_65569156dup , CM000676.1:g.65569155_65569156dup	GRCh37
NC_000014.7:g.64638908_64638909dup	NCBI36
NG_029830.1:g.5077_5078dup , LRG_530:g.5077_5078dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000556892.6:c.-157+76_-157+77dup	ENSP00000452206.2:n.-157+76_-157+77dup
ENST00000556979.6:c.-94_-93dup	ENSP00000452378.1:n.-94_-93dup
ENST00000358664.9:c.-94_-93dup MANE Select	ENSP00000351490.4:n.-94_-93dup
ENST00000246163.2:c.-94_-93dup	ENSP00000246163.2:n.-94_-93dup
ENST00000284165.10:c.-94_-93dup	ENSP00000284165.6:n.-94_-93dup
ENST00000358402.8:c.-94_-93dup	ENSP00000351175.4:n.-94_-93dup
ENST00000358664.8:c.-94_-93dup	ENSP00000351490.4:n.-94_-93dup
ENST00000394606.6:c.-94_-93dup	ENSP00000378104.2:n.-94_-93dup
ENST00000554709.1:n.85_86dup
ENST00000555667.5:c.-94_-93dup	ENSP00000452286.1:n.-94_-93dup
ENST00000555932.5:c.-94_-93dup	ENSP00000450763.1:n.-94_-93dup
ENST00000556443.5:c.-94_-93dup	ENSP00000450818.1:n.-94_-93dup
ENST00000556702.1:n.46_47dup
ENST00000556892.5:c.-157+76_-157+77dup	ENSP00000452206.1:n.-157+76_-157+77dup
ENST00000556979.5:c.-94_-93dup	ENSP00000452378.1:n.-94_-93dup
ENST00000557277.5:c.-239+76_-239+77dup	ENSP00000450955.1:n.-239+76_-239+77dup
ENST00000557746.5:c.-94_-93dup	ENSP00000452197.1:n.-94_-93dup
ENST00000618858.4:c.-94_-93dup	ENSP00000480127.1:n.-94_-93dup
NM_001271068.1:c.-94_-93dup	NP_001257997.1:n.-94_-93dup
NM_001271069.1:c.-94_-93dup	NP_001257998.1:n.-94_-93dup
NM_002382.4:c.-94_-93dup	NP_002373.3:n.-94_-93dup
NM_145112.2:c.-94_-93dup	NP_660087.1:n.-94_-93dup
NM_145113.2:c.-94_-93dup	NP_660088.1:n.-94_-93dup
NM_145114.2:c.-94_-93dup	NP_660089.1:n.-94_-93dup
NM_197957.3:c.-94_-93dup	NP_932061.1:n.-94_-93dup
NR_073137.1:n.187+76_187+77dup
NR_073138.1:n.187+76_187+77dup
XM_011536773.1:c.-94_-93dup	XP_011535075.1:n.-94_-93dup
XR_429315.2:n.109_110dup
XR_943450.1:n.109_110dup
XR_943451.1:n.109_110dup
XR_943452.1:n.98_99dup
NM_001320415.1:c.-368_-367dup	NP_001307344.1:n.-368_-367dup
XM_011536773.3:c.-94_-93dup	XP_011535075.1:n.-94_-93dup
XM_017021312.2:c.-341_-340dup	XP_016876801.1:n.-341_-340dup
XR_001750326.2:n.97_98dup
XR_001750327.2:n.97_98dup
XR_002957553.1:n.100_101dup
XR_943450.3:n.109_110dup
XR_943451.3:n.109_110dup
XR_943452.3:n.97_98dup
NM_001320415.2:c.-368_-367dup	NP_001307344.1:n.-368_-367dup
NM_002382.5:c.-94_-93dup MANE Select	NP_002373.3:n.-94_-93dup
NM_145112.3:c.-94_-93dup	NP_660087.1:n.-94_-93dup
NM_145113.3:c.-94_-93dup	NP_660088.1:n.-94_-93dup
NM_001271068.2:c.-94_-93dup	NP_001257997.1:n.-94_-93dup
NM_001271069.2:c.-94_-93dup	NP_001257998.1:n.-94_-93dup
NM_145114.3:c.-94_-93dup	NP_660089.1:n.-94_-93dup
NM_197957.4:c.-94_-93dup	NP_932061.1:n.-94_-93dup