Canonical Allele Identifier: CA971330887
Gene: HEXA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72347303_72347304insGCTCTGTC , CM000677.2:g.72347303_72347304insGCTCTGTC GRCh38
NC_000015.9:g.72639644_72639645insGCTCTGTC , CM000677.1:g.72639644_72639645insGCTCTGTC GRCh37
NC_000015.8:g.70426698_70426699insGCTCTGTC NCBI36
NG_009017.1:g.33878_33879insCAGAGCGA
NG_009017.2:g.33878_33879insCAGAGCGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.1073+746_1073+747insCAGAGCGA ENSP00000457521.2:n.1073+746_1073+747insCAGAGCGA
ENST00000682061.1:c.*808+384_*808+385insCAGAGCGA ENSP00000508316.1:n.*808+384_*808+385insCAGAGCGA
ENST00000682177.1:c.1189+384_1189+385insCAGAGCGA ENSP00000507409.1:n.1189+384_1189+385insCAGAGCGA
ENST00000682461.1:c.1252+384_1252+385insCAGAGCGA ENSP00000507308.1:n.1252+384_1252+385insCAGAGCGA
ENST00000682653.1:n.1466+384_1466+385insCAGAGCGA
ENST00000682657.1:c.*483+746_*483+747insCAGAGCGA ENSP00000507753.1:n.*483+746_*483+747insCAGAGCGA
ENST00000682721.1:c.*949+384_*949+385insCAGAGCGA ENSP00000507535.1:n.*949+384_*949+385insCAGAGCGA
ENST00000682843.1:c.*971+746_*971+747insCAGAGCGA ENSP00000508173.1:n.*971+746_*971+747insCAGAGCGA
ENST00000683003.1:c.*483+746_*483+747insCAGAGCGA ENSP00000507576.1:n.*483+746_*483+747insCAGAGCGA
ENST00000683133.1:c.1330+384_1330+385insCAGAGCGA ENSP00000508108.1:n.1330+384_1330+385insCAGAGCGA
ENST00000683228.1:n.1561_1562insCAGAGCGA
ENST00000683243.1:c.*483+746_*483+747insCAGAGCGA ENSP00000507042.1:n.*483+746_*483+747insCAGAGCGA
ENST00000683463.1:c.1074-592_1074-591insCAGAGCGA ENSP00000507986.1:n.1074-592_1074-591insCAGAGCGA
ENST00000683548.1:n.1104+746_1104+747insCAGAGCGA
ENST00000683579.1:c.*1044+384_*1044+385insCAGAGCGA ENSP00000506867.1:n.*1044+384_*1044+385insCAGAGCGA
ENST00000683587.1:n.1177+384_1177+385insCAGAGCGA
ENST00000683681.1:c.1146+384_1146+385insCAGAGCGA ENSP00000508110.1:n.1146+384_1146+385insCAGAGCGA
ENST00000683735.1:c.*1044+384_*1044+385insCAGAGCGA ENSP00000508336.1:n.*1044+384_*1044+385insCAGAGCGA
ENST00000683742.1:n.1361_1362insCAGAGCGA
ENST00000683853.1:c.1074-592_1074-591insCAGAGCGA ENSP00000506834.1:n.1074-592_1074-591insCAGAGCGA
ENST00000683860.1:c.1146+384_1146+385insCAGAGCGA ENSP00000507179.1:n.1146+384_1146+385insCAGAGCGA
ENST00000683884.1:c.1146+384_1146+385insCAGAGCGA ENSP00000507004.1:n.1146+384_1146+385insCAGAGCGA
ENST00000684041.1:c.1146+384_1146+385insCAGAGCGA ENSP00000508382.1:n.1146+384_1146+385insCAGAGCGA
ENST00000684125.1:c.1073+746_1073+747insCAGAGCGA ENSP00000507320.1:n.1073+746_1073+747insCAGAGCGA
ENST00000684203.1:n.2912-592_2912-591insCAGAGCGA
ENST00000684231.1:c.*556+384_*556+385insCAGAGCGA ENSP00000507748.1:n.*556+384_*556+385insCAGAGCGA
ENST00000684263.1:c.*86+384_*86+385insCAGAGCGA ENSP00000508369.1:n.*86+384_*86+385insCAGAGCGA
ENST00000684305.1:c.1594+384_1594+385insCAGAGCGA ENSP00000506819.1:n.1594+384_1594+385insCAGAGCGA
ENST00000684415.1:c.*14-592_*14-591insCAGAGCGA ENSP00000507227.1:n.*14-592_*14-591insCAGAGCGA
ENST00000684520.1:c.1146+384_1146+385insCAGAGCGA ENSP00000506826.1:n.1146+384_1146+385insCAGAGCGA
ENST00000684602.1:c.*812+384_*812+385insCAGAGCGA ENSP00000507996.1:n.*812+384_*812+385insCAGAGCGA
ENST00000684667.1:c.1477+384_1477+385insCAGAGCGA ENSP00000507003.1:n.1477+384_1477+385insCAGAGCGA
ENST00000268097.10:c.1146+384_1146+385insCAGAGCGA MANE Select ENSP00000268097.6:n.1146+384_1146+385insCAGAGCGA
ENST00000268097.9:c.1146+384_1146+385insCAGAGCGA ENSP00000268097.5:n.1146+384_1146+385insCAGAGCGA
ENST00000379915.4:c.413-977_413-976insCAGAGCGA ENSP00000478716.1:n.413-977_413-976insCAGAGCGA
ENST00000563762.5:c.825+746_825+747insCAGAGCGA ENSP00000456346.1:n.825+746_825+747insCAGAGCGA
ENST00000566304.5:c.1179+384_1179+385insCAGAGCGA ENSP00000455114.1:n.1179+384_1179+385insCAGAGCGA
ENST00000566672.5:c.*556+384_*556+385insCAGAGCGA ENSP00000457037.1:n.*556+384_*556+385insCAGAGCGA
ENST00000567027.5:c.945+746_945+747insCAGAGCGA
ENST00000567159.5:c.1146+384_1146+385insCAGAGCGA ENSP00000456489.1:n.1146+384_1146+385insCAGAGCGA
ENST00000567411.5:c.*667+384_*667+385insCAGAGCGA ENSP00000455545.1:n.*667+384_*667+385insCAGAGCGA
ENST00000568777.5:n.6550+384_6550+385insCAGAGCGA
ENST00000569410.5:c.1074-592_1074-591insCAGAGCGA ENSP00000457125.1:n.1074-592_1074-591insCAGAGCGA
NM_000520.4:c.1146+384_1146+385insCAGAGCGA NP_000511.2:n.1146+384_1146+385insCAGAGCGA
NM_000520.5:c.1146+384_1146+385insCAGAGCGA NP_000511.2:n.1146+384_1146+385insCAGAGCGA
NM_001318825.1:c.1179+384_1179+385insCAGAGCGA NP_001305754.1:n.1179+384_1179+385insCAGAGCGA
NR_134869.1:n.1574+746_1574+747insCAGAGCGA
NM_000520.6:c.1146+384_1146+385insCAGAGCGA MANE Select NP_000511.2:n.1146+384_1146+385insCAGAGCGA
NM_001318825.2:c.1179+384_1179+385insCAGAGCGA NP_001305754.1:n.1179+384_1179+385insCAGAGCGA
NR_134869.2:n.1115+746_1115+747insCAGAGCGA
NR_134869.3:n.1115+746_1115+747insCAGAGCGA