Canonical Allele Identifier: CA393062445

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72641503C>G (hg19) ; chr15:g.72349162C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72349162C>G , CM000677.2:g.72349162C>G	GRCh38
NC_000015.9:g.72641503C>G , CM000677.1:g.72641503C>G	GRCh37
NC_000015.8:g.70428557C>G	NCBI36
NG_009017.1:g.32018G>C
NG_009017.2:g.32018G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000563908.2:n.3249G>C
ENST00000567027.6:c.903G>C	ENSP00000457521.2:p.Met301Ile
ENST00000682061.1:c.*565G>C	ENSP00000508316.1:n.*565G>C
ENST00000682177.1:c.946G>C	ENSP00000507409.1:n.946G>C
ENST00000682461.1:c.1009G>C	ENSP00000507308.1:n.1009G>C
ENST00000682653.1:n.934G>C
ENST00000682657.1:c.*313G>C	ENSP00000507753.1:n.*313G>C
ENST00000682721.1:c.*706G>C	ENSP00000507535.1:n.*706G>C
ENST00000682843.1:c.*801G>C	ENSP00000508173.1:n.*801G>C
ENST00000683003.1:c.*313G>C	ENSP00000507576.1:n.*313G>C
ENST00000683133.1:c.1087G>C	ENSP00000508108.1:n.1087G>C
ENST00000683228.1:n.934G>C
ENST00000683243.1:c.*313G>C	ENSP00000507042.1:n.*313G>C
ENST00000683463.1:c.903G>C	ENSP00000507986.1:p.Met301Ile
ENST00000683548.1:n.934G>C
ENST00000683579.1:c.*801G>C	ENSP00000506867.1:n.*801G>C
ENST00000683587.1:n.934G>C
ENST00000683681.1:c.903G>C	ENSP00000508110.1:p.Met301Ile
ENST00000683735.1:c.*801G>C	ENSP00000508336.1:n.*801G>C
ENST00000683742.1:n.734G>C
ENST00000683853.1:c.903G>C	ENSP00000506834.1:p.Met301Ile
ENST00000683860.1:c.903G>C	ENSP00000507179.1:p.Met301Ile
ENST00000683884.1:c.903G>C	ENSP00000507004.1:p.Met301Ile
ENST00000684041.1:c.903G>C	ENSP00000508382.1:p.Met301Ile
ENST00000684125.1:c.903G>C	ENSP00000507320.1:p.Met301Ile
ENST00000684203.1:n.2741G>C
ENST00000684231.1:c.*313G>C	ENSP00000507748.1:n.*313G>C
ENST00000684263.1:c.903G>C	ENSP00000508369.1:p.Met301Ile
ENST00000684305.1:c.1351G>C	ENSP00000506819.1:n.1351G>C
ENST00000684415.1:c.903G>C	ENSP00000507227.1:p.Met301Ile
ENST00000684520.1:c.903G>C	ENSP00000506826.1:p.Met301Ile
ENST00000684602.1:c.*569G>C	ENSP00000507996.1:n.*569G>C
ENST00000684667.1:c.1234G>C	ENSP00000507003.1:n.1234G>C
ENST00000268097.10:c.903G>C MANE Select	ENSP00000268097.6:p.Met301Ile
ENST00000268097.9:c.903G>C	ENSP00000268097.5:p.Met301Ile
ENST00000379915.4:c.413-2837G>C	ENSP00000478716.1:n.413-2837G>C
ENST00000563762.5:c.739-1028G>C	ENSP00000456346.1:n.739-1028G>C
ENST00000566304.5:c.936G>C	ENSP00000455114.1:p.Met312Ile
ENST00000566672.5:c.*313G>C	ENSP00000457037.1:n.*313G>C
ENST00000567027.5:c.775G>C
ENST00000567159.5:c.903G>C	ENSP00000456489.1:p.Met301Ile
ENST00000567411.5:c.*424G>C	ENSP00000455545.1:n.*424G>C
ENST00000568777.5:n.6307G>C
ENST00000569410.5:c.903G>C	ENSP00000457125.1:p.Met301Ile
NM_000520.4:c.903G>C	NP_000511.2:p.Met301Ile
NM_000520.5:c.903G>C	NP_000511.2:p.Met301Ile
NM_001318825.1:c.936G>C	NP_001305754.1:p.Met312Ile
NR_134869.1:n.1404G>C
NM_000520.6:c.903G>C MANE Select	NP_000511.2:p.Met301Ile
NM_001318825.2:c.936G>C	NP_001305754.1:p.Met312Ile
NR_134869.2:n.945G>C
NR_134869.3:n.945G>C