Canonical Allele Identifier: CA393061261

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72639014T>A (hg19) ; chr15:g.72346673T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72346673T>A , CM000677.2:g.72346673T>A	GRCh38
NC_000015.9:g.72639014T>A , CM000677.1:g.72639014T>A	GRCh37
NC_000015.8:g.70426068T>A	NCBI36
NG_009017.1:g.34507A>T
NG_009017.2:g.34507A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.1074-348A>T	ENSP00000457521.2:n.1074-348A>T
ENST00000682061.1:c.*846A>T	ENSP00000508316.1:n.*846A>T
ENST00000682064.1:n.526A>T
ENST00000682177.1:c.1227A>T	ENSP00000507409.1:n.1227A>T
ENST00000682235.1:n.523A>T
ENST00000682461.1:c.1290A>T	ENSP00000507308.1:n.1290A>T
ENST00000682653.1:n.1504A>T
ENST00000682657.1:c.*484-348A>T	ENSP00000507753.1:n.*484-348A>T
ENST00000682721.1:c.*987A>T	ENSP00000507535.1:n.*987A>T
ENST00000682843.1:c.*972-348A>T	ENSP00000508173.1:n.*972-348A>T
ENST00000683003.1:c.*484-348A>T	ENSP00000507576.1:n.*484-348A>T
ENST00000683133.1:c.1368A>T	ENSP00000508108.1:n.1368A>T
ENST00000683243.1:c.*484-348A>T	ENSP00000507042.1:n.*484-348A>T
ENST00000683463.1:c.1111A>T	ENSP00000507986.1:p.Ile371Leu
ENST00000683548.1:n.1105-348A>T
ENST00000683579.1:c.*1082A>T	ENSP00000506867.1:n.*1082A>T
ENST00000683587.1:n.1178-348A>T
ENST00000683681.1:c.1184A>T	ENSP00000508110.1:p.Asp395Val
ENST00000683735.1:c.*1045-348A>T	ENSP00000508336.1:n.*1045-348A>T
ENST00000683853.1:c.1111A>T	ENSP00000506834.1:p.Ile371Leu
ENST00000683860.1:c.1184A>T	ENSP00000507179.1:p.Asp395Val
ENST00000683884.1:c.1147-348A>T	ENSP00000507004.1:n.1147-348A>T
ENST00000684041.1:c.1184A>T	ENSP00000508382.1:p.Asp395Val
ENST00000684125.1:c.1074-348A>T	ENSP00000507320.1:n.1074-348A>T
ENST00000684203.1:n.2949A>T
ENST00000684231.1:c.*594A>T	ENSP00000507748.1:n.*594A>T
ENST00000684263.1:c.*124A>T	ENSP00000508369.1:n.*124A>T
ENST00000684305.1:c.1632A>T	ENSP00000506819.1:n.1632A>T
ENST00000684415.1:c.*51A>T	ENSP00000507227.1:n.*51A>T
ENST00000684520.1:c.1184A>T	ENSP00000506826.1:p.Asp395Val
ENST00000684602.1:c.*850A>T	ENSP00000507996.1:n.*850A>T
ENST00000684667.1:c.1515A>T	ENSP00000507003.1:n.1515A>T
ENST00000268097.10:c.1184A>T MANE Select	ENSP00000268097.6:p.Asp395Val
ENST00000268097.9:c.1184A>T	ENSP00000268097.5:p.Asp395Val
ENST00000379915.4:c.413-348A>T	ENSP00000478716.1:n.413-348A>T
ENST00000563762.5:c.826-348A>T	ENSP00000456346.1:n.826-348A>T
ENST00000566304.5:c.1217A>T	ENSP00000455114.1:p.Asp406Val
ENST00000566672.5:c.*594A>T	ENSP00000457037.1:n.*594A>T
ENST00000567027.5:c.946-348A>T
ENST00000567159.5:c.1184A>T	ENSP00000456489.1:p.Asp395Val
ENST00000567411.5:c.*705A>T	ENSP00000455545.1:n.*705A>T
ENST00000568777.5:n.6551-348A>T
ENST00000569410.5:c.1111A>T	ENSP00000457125.1:p.Ile371Leu
NM_000520.4:c.1184A>T	NP_000511.2:p.Asp395Val
NM_000520.5:c.1184A>T	NP_000511.2:p.Asp395Val
NM_001318825.1:c.1217A>T	NP_001305754.1:p.Asp406Val
NR_134869.1:n.1575-348A>T
NM_000520.6:c.1184A>T MANE Select	NP_000511.2:p.Asp395Val
NM_001318825.2:c.1217A>T	NP_001305754.1:p.Asp406Val
NR_134869.2:n.1116-348A>T
NR_134869.3:n.1116-348A>T