Canonical Allele Identifier: CA971330879

Gene: HEXA

Linked Data

• gnomAD v3: 15-72347293-G-GAC
• gnomAD v4: 15-72347293-G-GAC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72347293_72347294insAC , CM000677.2:g.72347293_72347294insAC	GRCh38
NC_000015.9:g.72639634_72639635insAC , CM000677.1:g.72639634_72639635insAC	GRCh37
NC_000015.8:g.70426688_70426689insAC	NCBI36
NG_009017.1:g.33886_33887insGT
NG_009017.2:g.33886_33887insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.1073+754_1073+755insGT	ENSP00000457521.2:n.1073+754_1073+755insGT
ENST00000682061.1:c.*808+392_*808+393insGT	ENSP00000508316.1:n.*808+392_*808+393insGT
ENST00000682177.1:c.1189+392_1189+393insGT	ENSP00000507409.1:n.1189+392_1189+393insGT
ENST00000682461.1:c.1252+392_1252+393insGT	ENSP00000507308.1:n.1252+392_1252+393insGT
ENST00000682653.1:n.1466+392_1466+393insGT
ENST00000682657.1:c.*483+754_*483+755insGT	ENSP00000507753.1:n.*483+754_*483+755insGT
ENST00000682721.1:c.*949+392_*949+393insGT	ENSP00000507535.1:n.*949+392_*949+393insGT
ENST00000682843.1:c.*971+754_*971+755insGT	ENSP00000508173.1:n.*971+754_*971+755insGT
ENST00000683003.1:c.*483+754_*483+755insGT	ENSP00000507576.1:n.*483+754_*483+755insGT
ENST00000683133.1:c.1330+392_1330+393insGT	ENSP00000508108.1:n.1330+392_1330+393insGT
ENST00000683228.1:n.1569_1570insGT
ENST00000683243.1:c.*483+754_*483+755insGT	ENSP00000507042.1:n.*483+754_*483+755insGT
ENST00000683463.1:c.1074-584_1074-583insGT	ENSP00000507986.1:n.1074-584_1074-583insGT
ENST00000683548.1:n.1104+754_1104+755insGT
ENST00000683579.1:c.*1044+392_*1044+393insGT	ENSP00000506867.1:n.*1044+392_*1044+393insGT
ENST00000683587.1:n.1177+392_1177+393insGT
ENST00000683681.1:c.1146+392_1146+393insGT	ENSP00000508110.1:n.1146+392_1146+393insGT
ENST00000683735.1:c.*1044+392_*1044+393insGT	ENSP00000508336.1:n.*1044+392_*1044+393insGT
ENST00000683742.1:n.1369_1370insGT
ENST00000683853.1:c.1074-584_1074-583insGT	ENSP00000506834.1:n.1074-584_1074-583insGT
ENST00000683860.1:c.1146+392_1146+393insGT	ENSP00000507179.1:n.1146+392_1146+393insGT
ENST00000683884.1:c.1146+392_1146+393insGT	ENSP00000507004.1:n.1146+392_1146+393insGT
ENST00000684041.1:c.1146+392_1146+393insGT	ENSP00000508382.1:n.1146+392_1146+393insGT
ENST00000684125.1:c.1073+754_1073+755insGT	ENSP00000507320.1:n.1073+754_1073+755insGT
ENST00000684203.1:n.2912-584_2912-583insGT
ENST00000684231.1:c.*556+392_*556+393insGT	ENSP00000507748.1:n.*556+392_*556+393insGT
ENST00000684263.1:c.*86+392_*86+393insGT	ENSP00000508369.1:n.*86+392_*86+393insGT
ENST00000684305.1:c.1594+392_1594+393insGT	ENSP00000506819.1:n.1594+392_1594+393insGT
ENST00000684415.1:c.*14-584_*14-583insGT	ENSP00000507227.1:n.*14-584_*14-583insGT
ENST00000684520.1:c.1146+392_1146+393insGT	ENSP00000506826.1:n.1146+392_1146+393insGT
ENST00000684602.1:c.*812+392_*812+393insGT	ENSP00000507996.1:n.*812+392_*812+393insGT
ENST00000684667.1:c.1477+392_1477+393insGT	ENSP00000507003.1:n.1477+392_1477+393insGT
ENST00000268097.10:c.1146+392_1146+393insGT MANE Select	ENSP00000268097.6:n.1146+392_1146+393insGT
ENST00000268097.9:c.1146+392_1146+393insGT	ENSP00000268097.5:n.1146+392_1146+393insGT
ENST00000379915.4:c.413-969_413-968insGT	ENSP00000478716.1:n.413-969_413-968insGT
ENST00000563762.5:c.825+754_825+755insGT	ENSP00000456346.1:n.825+754_825+755insGT
ENST00000566304.5:c.1179+392_1179+393insGT	ENSP00000455114.1:n.1179+392_1179+393insGT
ENST00000566672.5:c.*556+392_*556+393insGT	ENSP00000457037.1:n.*556+392_*556+393insGT
ENST00000567027.5:c.945+754_945+755insGT
ENST00000567159.5:c.1146+392_1146+393insGT	ENSP00000456489.1:n.1146+392_1146+393insGT
ENST00000567411.5:c.*667+392_*667+393insGT	ENSP00000455545.1:n.*667+392_*667+393insGT
ENST00000568777.5:n.6550+392_6550+393insGT
ENST00000569410.5:c.1074-584_1074-583insGT	ENSP00000457125.1:n.1074-584_1074-583insGT
NM_000520.4:c.1146+392_1146+393insGT	NP_000511.2:n.1146+392_1146+393insGT
NM_000520.5:c.1146+392_1146+393insGT	NP_000511.2:n.1146+392_1146+393insGT
NM_001318825.1:c.1179+392_1179+393insGT	NP_001305754.1:n.1179+392_1179+393insGT
NR_134869.1:n.1574+754_1574+755insGT
NM_000520.6:c.1146+392_1146+393insGT MANE Select	NP_000511.2:n.1146+392_1146+393insGT
NM_001318825.2:c.1179+392_1179+393insGT	NP_001305754.1:n.1179+392_1179+393insGT
NR_134869.2:n.1115+754_1115+755insGT
NR_134869.3:n.1115+754_1115+755insGT