Canonical Allele Identifier: CA2575554692

Gene: MAX

Linked Data

• gnomAD v4: 14-65102447-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65102449_65102450del , CM000676.2:g.65102449_65102450del	GRCh38
NC_000014.8:g.65569167_65569168del , CM000676.1:g.65569167_65569168del	GRCh37
NC_000014.7:g.64638920_64638921del	NCBI36
NG_029830.1:g.5061_5062del , LRG_530:g.5061_5062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.-157+60_-157+61del	ENSP00000452206.2:n.-157+60_-157+61del
ENST00000556979.6:c.-110_-109del	ENSP00000452378.1:n.-110_-109del
ENST00000358664.9:c.-110_-109del MANE Select	ENSP00000351490.4:n.-110_-109del
ENST00000246163.2:c.-110_-109del	ENSP00000246163.2:n.-110_-109del
ENST00000284165.10:c.-110_-109del	ENSP00000284165.6:n.-110_-109del
ENST00000358402.8:c.-110_-109del	ENSP00000351175.4:n.-110_-109del
ENST00000358664.8:c.-110_-109del	ENSP00000351490.4:n.-110_-109del
ENST00000394606.6:c.-110_-109del	ENSP00000378104.2:n.-110_-109del
ENST00000554709.1:n.69_70del
ENST00000555667.5:c.-110_-109del	ENSP00000452286.1:n.-110_-109del
ENST00000555932.5:c.-110_-109del	ENSP00000450763.1:n.-110_-109del
ENST00000556443.5:c.-110_-109del	ENSP00000450818.1:n.-110_-109del
ENST00000556702.1:n.30_31del
ENST00000556892.5:c.-157+60_-157+61del	ENSP00000452206.1:n.-157+60_-157+61del
ENST00000556979.5:c.-110_-109del	ENSP00000452378.1:n.-110_-109del
ENST00000557277.5:c.-239+60_-239+61del	ENSP00000450955.1:n.-239+60_-239+61del
ENST00000557746.5:c.-110_-109del	ENSP00000452197.1:n.-110_-109del
ENST00000618858.4:c.-110_-109del	ENSP00000480127.1:n.-110_-109del
NM_001271068.1:c.-110_-109del	NP_001257997.1:n.-110_-109del
NM_001271069.1:c.-110_-109del	NP_001257998.1:n.-110_-109del
NM_002382.4:c.-110_-109del	NP_002373.3:n.-110_-109del
NM_145112.2:c.-110_-109del	NP_660087.1:n.-110_-109del
NM_145113.2:c.-110_-109del	NP_660088.1:n.-110_-109del
NM_145114.2:c.-110_-109del	NP_660089.1:n.-110_-109del
NM_197957.3:c.-110_-109del	NP_932061.1:n.-110_-109del
NR_073137.1:n.187+60_187+61del
NR_073138.1:n.187+60_187+61del
XM_011536773.1:c.-110_-109del	XP_011535075.1:n.-110_-109del
XR_429315.2:n.93_94del
XR_943450.1:n.93_94del
XR_943451.1:n.93_94del
XR_943452.1:n.82_83del
NM_001320415.1:c.-384_-383del	NP_001307344.1:n.-384_-383del
XM_011536773.3:c.-110_-109del	XP_011535075.1:n.-110_-109del
XM_017021312.2:c.-357_-356del	XP_016876801.1:n.-357_-356del
XR_001750326.2:n.81_82del
XR_001750327.2:n.81_82del
XR_002957553.1:n.84_85del
XR_943450.3:n.93_94del
XR_943451.3:n.93_94del
XR_943452.3:n.81_82del
NM_001320415.2:c.-384_-383del	NP_001307344.1:n.-384_-383del
NM_002382.5:c.-110_-109del MANE Select	NP_002373.3:n.-110_-109del
NM_145112.3:c.-110_-109del	NP_660087.1:n.-110_-109del
NM_145113.3:c.-110_-109del	NP_660088.1:n.-110_-109del
NM_001271068.2:c.-110_-109del	NP_001257997.1:n.-110_-109del
NM_001271069.2:c.-110_-109del	NP_001257998.1:n.-110_-109del
NM_145114.3:c.-110_-109del	NP_660089.1:n.-110_-109del
NM_197957.4:c.-110_-109del	NP_932061.1:n.-110_-109del