Canonical Allele Identifier: CA393059398

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72638661G>T (hg19) ; chr15:g.72346320G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72346320G>T , CM000677.2:g.72346320G>T	GRCh38
NC_000015.9:g.72638661G>T , CM000677.1:g.72638661G>T	GRCh37
NC_000015.8:g.70425715G>T	NCBI36
NG_009017.1:g.34860C>A
NG_009017.2:g.34860C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.1079C>A	ENSP00000457521.2:p.Pro360His
ENST00000682061.1:c.*998C>A	ENSP00000508316.1:n.*998C>A
ENST00000682064.1:n.879C>A
ENST00000682177.1:c.1379C>A	ENSP00000507409.1:n.1379C>A
ENST00000682235.1:n.675C>A
ENST00000682461.1:c.1442C>A	ENSP00000507308.1:n.1442C>A
ENST00000682653.1:n.1656C>A
ENST00000682657.1:c.*489C>A	ENSP00000507753.1:n.*489C>A
ENST00000682721.1:c.*1139C>A	ENSP00000507535.1:n.*1139C>A
ENST00000682843.1:c.*977C>A	ENSP00000508173.1:n.*977C>A
ENST00000683003.1:c.*489C>A	ENSP00000507576.1:n.*489C>A
ENST00000683133.1:c.1520C>A	ENSP00000508108.1:n.1520C>A
ENST00000683243.1:c.*489C>A	ENSP00000507042.1:n.*489C>A
ENST00000683463.1:c.*141C>A	ENSP00000507986.1:n.*141C>A
ENST00000683548.1:n.1110C>A
ENST00000683579.1:c.*1234C>A	ENSP00000506867.1:n.*1234C>A
ENST00000683587.1:n.1183C>A
ENST00000683681.1:c.1336C>A	ENSP00000508110.1:p.Pro446Thr
ENST00000683735.1:c.*1050C>A	ENSP00000508336.1:n.*1050C>A
ENST00000683853.1:c.*141C>A	ENSP00000506834.1:n.*141C>A
ENST00000683860.1:c.1336C>A	ENSP00000507179.1:p.Pro446Thr
ENST00000683884.1:c.1152C>A	ENSP00000507004.1:p.Pro384=
ENST00000684041.1:c.1336C>A	ENSP00000508382.1:p.Pro446Thr
ENST00000684125.1:c.1079C>A	ENSP00000507320.1:p.Pro360His
ENST00000684203.1:n.3101C>A
ENST00000684231.1:c.*746C>A	ENSP00000507748.1:n.*746C>A
ENST00000684263.1:c.*276C>A	ENSP00000508369.1:n.*276C>A
ENST00000684305.1:c.1784C>A	ENSP00000506819.1:n.1784C>A
ENST00000684415.1:c.*203C>A	ENSP00000507227.1:n.*203C>A
ENST00000684520.1:c.1336C>A	ENSP00000506826.1:p.Pro446Thr
ENST00000684602.1:c.*1002C>A	ENSP00000507996.1:n.*1002C>A
ENST00000684667.1:c.1667C>A	ENSP00000507003.1:n.1667C>A
ENST00000268097.10:c.1336C>A MANE Select	ENSP00000268097.6:p.Pro446Thr
ENST00000268097.9:c.1336C>A	ENSP00000268097.5:p.Pro446Thr
ENST00000379915.4:c.418C>A	ENSP00000478716.1:p.Pro140Thr
ENST00000563762.5:c.831C>A	ENSP00000456346.1:n.831C>A
ENST00000566304.5:c.1369C>A	ENSP00000455114.1:p.Pro457Thr
ENST00000566672.5:c.*746C>A	ENSP00000457037.1:n.*746C>A
ENST00000567027.5:c.951C>A
ENST00000567159.5:c.1336C>A	ENSP00000456489.1:p.Pro446Thr
ENST00000567411.5:c.*857C>A	ENSP00000455545.1:n.*857C>A
ENST00000568777.5:n.6556C>A
ENST00000569410.5:c.*141C>A	ENSP00000457125.1:n.*141C>A
NM_000520.4:c.1336C>A	NP_000511.2:p.Pro446Thr
NM_000520.5:c.1336C>A	NP_000511.2:p.Pro446Thr
NM_001318825.1:c.1369C>A	NP_001305754.1:p.Pro457Thr
NR_134869.1:n.1580C>A
NM_000520.6:c.1336C>A MANE Select	NP_000511.2:p.Pro446Thr
NM_001318825.2:c.1369C>A	NP_001305754.1:p.Pro457Thr
NR_134869.2:n.1121C>A
NR_134869.3:n.1121C>A