Canonical Allele Identifier: CA393061458

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72639044G>C (hg19) ; chr15:g.72346703G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72346703G>C , CM000677.2:g.72346703G>C	GRCh38
NC_000015.9:g.72639044G>C , CM000677.1:g.72639044G>C	GRCh37
NC_000015.8:g.70426098G>C	NCBI36
NG_009017.1:g.34477C>G
NG_009017.2:g.34477C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.1074-378C>G	ENSP00000457521.2:n.1074-378C>G
ENST00000682061.1:c.*816C>G	ENSP00000508316.1:n.*816C>G
ENST00000682064.1:n.496C>G
ENST00000682177.1:c.1197C>G	ENSP00000507409.1:n.1197C>G
ENST00000682235.1:n.493C>G
ENST00000682461.1:c.1260C>G	ENSP00000507308.1:n.1260C>G
ENST00000682653.1:n.1474C>G
ENST00000682657.1:c.*484-378C>G	ENSP00000507753.1:n.*484-378C>G
ENST00000682721.1:c.*957C>G	ENSP00000507535.1:n.*957C>G
ENST00000682843.1:c.*972-378C>G	ENSP00000508173.1:n.*972-378C>G
ENST00000683003.1:c.*484-378C>G	ENSP00000507576.1:n.*484-378C>G
ENST00000683133.1:c.1338C>G	ENSP00000508108.1:n.1338C>G
ENST00000683243.1:c.*484-378C>G	ENSP00000507042.1:n.*484-378C>G
ENST00000683463.1:c.1081C>G	ENSP00000507986.1:p.Gln361Glu
ENST00000683548.1:n.1105-378C>G
ENST00000683579.1:c.*1052C>G	ENSP00000506867.1:n.*1052C>G
ENST00000683587.1:n.1178-378C>G
ENST00000683681.1:c.1154C>G	ENSP00000508110.1:p.Pro385Arg
ENST00000683735.1:c.*1045-378C>G	ENSP00000508336.1:n.*1045-378C>G
ENST00000683853.1:c.1081C>G	ENSP00000506834.1:p.Gln361Glu
ENST00000683860.1:c.1154C>G	ENSP00000507179.1:p.Pro385Arg
ENST00000683884.1:c.1147-378C>G	ENSP00000507004.1:n.1147-378C>G
ENST00000684041.1:c.1154C>G	ENSP00000508382.1:p.Pro385Arg
ENST00000684125.1:c.1074-378C>G	ENSP00000507320.1:n.1074-378C>G
ENST00000684203.1:n.2919C>G
ENST00000684231.1:c.*564C>G	ENSP00000507748.1:n.*564C>G
ENST00000684263.1:c.*94C>G	ENSP00000508369.1:n.*94C>G
ENST00000684305.1:c.1602C>G	ENSP00000506819.1:n.1602C>G
ENST00000684415.1:c.*21C>G	ENSP00000507227.1:n.*21C>G
ENST00000684520.1:c.1154C>G	ENSP00000506826.1:p.Pro385Arg
ENST00000684602.1:c.*820C>G	ENSP00000507996.1:n.*820C>G
ENST00000684667.1:c.1485C>G	ENSP00000507003.1:n.1485C>G
ENST00000268097.10:c.1154C>G MANE Select	ENSP00000268097.6:p.Pro385Arg
ENST00000268097.9:c.1154C>G	ENSP00000268097.5:p.Pro385Arg
ENST00000379915.4:c.413-378C>G	ENSP00000478716.1:n.413-378C>G
ENST00000563762.5:c.826-378C>G	ENSP00000456346.1:n.826-378C>G
ENST00000566304.5:c.1187C>G	ENSP00000455114.1:p.Pro396Arg
ENST00000566672.5:c.*564C>G	ENSP00000457037.1:n.*564C>G
ENST00000567027.5:c.946-378C>G
ENST00000567159.5:c.1154C>G	ENSP00000456489.1:p.Pro385Arg
ENST00000567411.5:c.*675C>G	ENSP00000455545.1:n.*675C>G
ENST00000568777.5:n.6551-378C>G
ENST00000569410.5:c.1081C>G	ENSP00000457125.1:p.Gln361Glu
NM_000520.4:c.1154C>G	NP_000511.2:p.Pro385Arg
NM_000520.5:c.1154C>G	NP_000511.2:p.Pro385Arg
NM_001318825.1:c.1187C>G	NP_001305754.1:p.Pro396Arg
NR_134869.1:n.1575-378C>G
NM_000520.6:c.1154C>G MANE Select	NP_000511.2:p.Pro385Arg
NM_001318825.2:c.1187C>G	NP_001305754.1:p.Pro396Arg
NR_134869.2:n.1116-378C>G
NR_134869.3:n.1116-378C>G