Canonical Allele Identifier: CA393061753

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72640070T>G (hg19) ; chr15:g.72347729T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72347729T>G , CM000677.2:g.72347729T>G	GRCh38
NC_000015.9:g.72640070T>G , CM000677.1:g.72640070T>G	GRCh37
NC_000015.8:g.70427124T>G	NCBI36
NG_009017.1:g.33451A>C
NG_009017.2:g.33451A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.1073+319A>C	ENSP00000457521.2:n.1073+319A>C
ENST00000682061.1:c.*765A>C	ENSP00000508316.1:n.*765A>C
ENST00000682177.1:c.1146A>C	ENSP00000507409.1:n.1146A>C
ENST00000682461.1:c.1209A>C	ENSP00000507308.1:n.1209A>C
ENST00000682653.1:n.1423A>C
ENST00000682657.1:c.*483+319A>C	ENSP00000507753.1:n.*483+319A>C
ENST00000682721.1:c.*906A>C	ENSP00000507535.1:n.*906A>C
ENST00000682843.1:c.*971+319A>C	ENSP00000508173.1:n.*971+319A>C
ENST00000683003.1:c.*483+319A>C	ENSP00000507576.1:n.*483+319A>C
ENST00000683133.1:c.1287A>C	ENSP00000508108.1:n.1287A>C
ENST00000683228.1:n.1134A>C
ENST00000683243.1:c.*483+319A>C	ENSP00000507042.1:n.*483+319A>C
ENST00000683463.1:c.1073+319A>C	ENSP00000507986.1:n.1073+319A>C
ENST00000683548.1:n.1104+319A>C
ENST00000683579.1:c.*1001A>C	ENSP00000506867.1:n.*1001A>C
ENST00000683587.1:n.1134A>C
ENST00000683681.1:c.1103A>C	ENSP00000508110.1:p.Lys368Thr
ENST00000683735.1:c.*1001A>C	ENSP00000508336.1:n.*1001A>C
ENST00000683742.1:n.934A>C
ENST00000683853.1:c.1073+319A>C	ENSP00000506834.1:n.1073+319A>C
ENST00000683860.1:c.1103A>C	ENSP00000507179.1:p.Lys368Thr
ENST00000683884.1:c.1103A>C	ENSP00000507004.1:p.Lys368Thr
ENST00000684041.1:c.1103A>C	ENSP00000508382.1:p.Lys368Thr
ENST00000684125.1:c.1073+319A>C	ENSP00000507320.1:n.1073+319A>C
ENST00000684203.1:n.2911+319A>C
ENST00000684231.1:c.*513A>C	ENSP00000507748.1:n.*513A>C
ENST00000684263.1:c.*43A>C	ENSP00000508369.1:n.*43A>C
ENST00000684305.1:c.1551A>C	ENSP00000506819.1:n.1551A>C
ENST00000684415.1:c.*13+302A>C	ENSP00000507227.1:n.*13+302A>C
ENST00000684520.1:c.1103A>C	ENSP00000506826.1:p.Lys368Thr
ENST00000684602.1:c.*769A>C	ENSP00000507996.1:n.*769A>C
ENST00000684667.1:c.1434A>C	ENSP00000507003.1:n.1434A>C
ENST00000268097.10:c.1103A>C MANE Select	ENSP00000268097.6:p.Lys368Thr
ENST00000268097.9:c.1103A>C	ENSP00000268097.5:p.Lys368Thr
ENST00000379915.4:c.413-1404A>C	ENSP00000478716.1:n.413-1404A>C
ENST00000563762.5:c.825+319A>C	ENSP00000456346.1:n.825+319A>C
ENST00000566304.5:c.1136A>C	ENSP00000455114.1:p.Lys379Thr
ENST00000566672.5:c.*513A>C	ENSP00000457037.1:n.*513A>C
ENST00000567027.5:c.945+319A>C
ENST00000567159.5:c.1103A>C	ENSP00000456489.1:p.Lys368Thr
ENST00000567411.5:c.*624A>C	ENSP00000455545.1:n.*624A>C
ENST00000568777.5:n.6507A>C
ENST00000569410.5:c.1073+319A>C	ENSP00000457125.1:n.1073+319A>C
NM_000520.4:c.1103A>C	NP_000511.2:p.Lys368Thr
NM_000520.5:c.1103A>C	NP_000511.2:p.Lys368Thr
NM_001318825.1:c.1136A>C	NP_001305754.1:p.Lys379Thr
NR_134869.1:n.1574+319A>C
NM_000520.6:c.1103A>C MANE Select	NP_000511.2:p.Lys368Thr
NM_001318825.2:c.1136A>C	NP_001305754.1:p.Lys379Thr
NR_134869.2:n.1115+319A>C
NR_134869.3:n.1115+319A>C