Canonical Allele Identifier: CA7644760

Gene: HEXA

Linked Data

• ClinVar Variation Id: 555043
• ClinVar RCV Id: RCV000670783
• dbSNP Id: rs778878211
• ExAC: 15:72639009 G / A
• gnomAD v2: 15-72639009-G-A
• gnomAD v4: 15-72346668-G-A
• MyVariant Identifiers: chr15:g.72639009G>A (hg19) ; chr15:g.72346668G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72346668G>A , CM000677.2:g.72346668G>A	GRCh38
NC_000015.9:g.72639009G>A , CM000677.1:g.72639009G>A	GRCh37
NC_000015.8:g.70426063G>A	NCBI36
NG_009017.1:g.34512C>T
NG_009017.2:g.34512C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.1074-343C>T	ENSP00000457521.2:n.1074-343C>T
ENST00000682061.1:c.*851C>T	ENSP00000508316.1:n.*851C>T
ENST00000682064.1:n.531C>T
ENST00000682177.1:c.1232C>T	ENSP00000507409.1:n.1232C>T
ENST00000682235.1:n.528C>T
ENST00000682461.1:c.1295C>T	ENSP00000507308.1:n.1295C>T
ENST00000682653.1:n.1509C>T
ENST00000682657.1:c.*484-343C>T	ENSP00000507753.1:n.*484-343C>T
ENST00000682721.1:c.*992C>T	ENSP00000507535.1:n.*992C>T
ENST00000682843.1:c.*972-343C>T	ENSP00000508173.1:n.*972-343C>T
ENST00000683003.1:c.*484-343C>T	ENSP00000507576.1:n.*484-343C>T
ENST00000683133.1:c.1373C>T	ENSP00000508108.1:n.1373C>T
ENST00000683243.1:c.*484-343C>T	ENSP00000507042.1:n.*484-343C>T
ENST00000683463.1:c.1116C>T	ENSP00000507986.1:p.Phe372=
ENST00000683548.1:n.1105-343C>T
ENST00000683579.1:c.*1087C>T	ENSP00000506867.1:n.*1087C>T
ENST00000683587.1:n.1178-343C>T
ENST00000683681.1:c.1189C>T	ENSP00000508110.1:p.Pro397Ser
ENST00000683735.1:c.*1045-343C>T	ENSP00000508336.1:n.*1045-343C>T
ENST00000683853.1:c.1116C>T	ENSP00000506834.1:p.Phe372=
ENST00000683860.1:c.1189C>T	ENSP00000507179.1:p.Pro397Ser
ENST00000683884.1:c.1147-343C>T	ENSP00000507004.1:n.1147-343C>T
ENST00000684041.1:c.1189C>T	ENSP00000508382.1:p.Pro397Ser
ENST00000684125.1:c.1074-343C>T	ENSP00000507320.1:n.1074-343C>T
ENST00000684203.1:n.2954C>T
ENST00000684231.1:c.*599C>T	ENSP00000507748.1:n.*599C>T
ENST00000684263.1:c.*129C>T	ENSP00000508369.1:n.*129C>T
ENST00000684305.1:c.1637C>T	ENSP00000506819.1:n.1637C>T
ENST00000684415.1:c.*56C>T	ENSP00000507227.1:n.*56C>T
ENST00000684520.1:c.1189C>T	ENSP00000506826.1:p.Pro397Ser
ENST00000684602.1:c.*855C>T	ENSP00000507996.1:n.*855C>T
ENST00000684667.1:c.1520C>T	ENSP00000507003.1:n.1520C>T
ENST00000268097.10:c.1189C>T MANE Select	ENSP00000268097.6:p.Pro397Ser
ENST00000268097.9:c.1189C>T	ENSP00000268097.5:p.Pro397Ser
ENST00000379915.4:c.413-343C>T	ENSP00000478716.1:n.413-343C>T
ENST00000563762.5:c.826-343C>T	ENSP00000456346.1:n.826-343C>T
ENST00000566304.5:c.1222C>T	ENSP00000455114.1:p.Pro408Ser
ENST00000566672.5:c.*599C>T	ENSP00000457037.1:n.*599C>T
ENST00000567027.5:c.946-343C>T
ENST00000567159.5:c.1189C>T	ENSP00000456489.1:p.Pro397Ser
ENST00000567411.5:c.*710C>T	ENSP00000455545.1:n.*710C>T
ENST00000568777.5:n.6551-343C>T
ENST00000569410.5:c.1116C>T	ENSP00000457125.1:p.Phe372=
NM_000520.4:c.1189C>T	NP_000511.2:p.Pro397Ser
NM_000520.5:c.1189C>T	NP_000511.2:p.Pro397Ser
NM_001318825.1:c.1222C>T	NP_001305754.1:p.Pro408Ser
NR_134869.1:n.1575-343C>T
NM_000520.6:c.1189C>T MANE Select	NP_000511.2:p.Pro397Ser
NM_001318825.2:c.1222C>T	NP_001305754.1:p.Pro408Ser
NR_134869.2:n.1116-343C>T
NR_134869.3:n.1116-343C>T