Canonical Allele Identifier: CA393059405

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72638663G>T (hg19) ; chr15:g.72346322G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72346322G>T , CM000677.2:g.72346322G>T	GRCh38
NC_000015.9:g.72638663G>T , CM000677.1:g.72638663G>T	GRCh37
NC_000015.8:g.70425717G>T	NCBI36
NG_009017.1:g.34858C>A
NG_009017.2:g.34858C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.1077C>A	ENSP00000457521.2:p.Tyr359Ter
ENST00000682061.1:c.*996C>A	ENSP00000508316.1:n.*996C>A
ENST00000682064.1:n.877C>A
ENST00000682177.1:c.1377C>A	ENSP00000507409.1:n.1377C>A
ENST00000682235.1:n.673C>A
ENST00000682461.1:c.1440C>A	ENSP00000507308.1:n.1440C>A
ENST00000682653.1:n.1654C>A
ENST00000682657.1:c.*487C>A	ENSP00000507753.1:n.*487C>A
ENST00000682721.1:c.*1137C>A	ENSP00000507535.1:n.*1137C>A
ENST00000682843.1:c.*975C>A	ENSP00000508173.1:n.*975C>A
ENST00000683003.1:c.*487C>A	ENSP00000507576.1:n.*487C>A
ENST00000683133.1:c.1518C>A	ENSP00000508108.1:n.1518C>A
ENST00000683243.1:c.*487C>A	ENSP00000507042.1:n.*487C>A
ENST00000683463.1:c.*139C>A	ENSP00000507986.1:n.*139C>A
ENST00000683548.1:n.1108C>A
ENST00000683579.1:c.*1232C>A	ENSP00000506867.1:n.*1232C>A
ENST00000683587.1:n.1181C>A
ENST00000683681.1:c.1334C>A	ENSP00000508110.1:p.Thr445Asn
ENST00000683735.1:c.*1048C>A	ENSP00000508336.1:n.*1048C>A
ENST00000683853.1:c.*139C>A	ENSP00000506834.1:n.*139C>A
ENST00000683860.1:c.1334C>A	ENSP00000507179.1:p.Thr445Asn
ENST00000683884.1:c.1150C>A	ENSP00000507004.1:p.Pro384Thr
ENST00000684041.1:c.1334C>A	ENSP00000508382.1:p.Thr445Asn
ENST00000684125.1:c.1077C>A	ENSP00000507320.1:p.Tyr359Ter
ENST00000684203.1:n.3099C>A
ENST00000684231.1:c.*744C>A	ENSP00000507748.1:n.*744C>A
ENST00000684263.1:c.*274C>A	ENSP00000508369.1:n.*274C>A
ENST00000684305.1:c.1782C>A	ENSP00000506819.1:n.1782C>A
ENST00000684415.1:c.*201C>A	ENSP00000507227.1:n.*201C>A
ENST00000684520.1:c.1334C>A	ENSP00000506826.1:p.Thr445Asn
ENST00000684602.1:c.*1000C>A	ENSP00000507996.1:n.*1000C>A
ENST00000684667.1:c.1665C>A	ENSP00000507003.1:n.1665C>A
ENST00000268097.10:c.1334C>A MANE Select	ENSP00000268097.6:p.Thr445Asn
ENST00000268097.9:c.1334C>A	ENSP00000268097.5:p.Thr445Asn
ENST00000379915.4:c.416C>A	ENSP00000478716.1:p.Thr139Asn
ENST00000563762.5:c.829C>A	ENSP00000456346.1:n.829C>A
ENST00000566304.5:c.1367C>A	ENSP00000455114.1:p.Thr456Asn
ENST00000566672.5:c.*744C>A	ENSP00000457037.1:n.*744C>A
ENST00000567027.5:c.949C>A
ENST00000567159.5:c.1334C>A	ENSP00000456489.1:p.Thr445Asn
ENST00000567411.5:c.*855C>A	ENSP00000455545.1:n.*855C>A
ENST00000568777.5:n.6554C>A
ENST00000569410.5:c.*139C>A	ENSP00000457125.1:n.*139C>A
NM_000520.4:c.1334C>A	NP_000511.2:p.Thr445Asn
NM_000520.5:c.1334C>A	NP_000511.2:p.Thr445Asn
NM_001318825.1:c.1367C>A	NP_001305754.1:p.Thr456Asn
NR_134869.1:n.1578C>A
NM_000520.6:c.1334C>A MANE Select	NP_000511.2:p.Thr445Asn
NM_001318825.2:c.1367C>A	NP_001305754.1:p.Thr456Asn
NR_134869.2:n.1119C>A
NR_134869.3:n.1119C>A