Canonical Allele Identifier: CA491111987

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72637917A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72345576A>C , CM000677.2:g.72345576A>C	GRCh38
NC_000015.9:g.72637917A>C , CM000677.1:g.72637917A>C	GRCh37
NC_000015.8:g.70424971A>C	NCBI36
NG_009017.1:g.35604T>G
NG_009017.2:g.35604T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.*82-26T>G	ENSP00000457521.2:n.*82-26T>G
ENST00000682061.1:c.*1742T>G	ENSP00000508316.1:n.*1742T>G
ENST00000682064.1:n.1623T>G
ENST00000682177.1:c.1465-26T>G	ENSP00000507409.1:n.1465-26T>G
ENST00000682235.1:n.1419T>G
ENST00000682461.1:c.1528-26T>G	ENSP00000507308.1:n.1528-26T>G
ENST00000682653.1:n.2400T>G
ENST00000682657.1:c.*1233T>G	ENSP00000507753.1:n.*1233T>G
ENST00000682721.1:c.*1225-26T>G	ENSP00000507535.1:n.*1225-26T>G
ENST00000682843.1:c.*1063-26T>G	ENSP00000508173.1:n.*1063-26T>G
ENST00000683003.1:c.*1233T>G	ENSP00000507576.1:n.*1233T>G
ENST00000683133.1:c.1606-26T>G	ENSP00000508108.1:n.1606-26T>G
ENST00000683243.1:c.*575-26T>G	ENSP00000507042.1:n.*575-26T>G
ENST00000683463.1:c.*885T>G	ENSP00000507986.1:n.*885T>G
ENST00000683548.1:n.1854T>G
ENST00000683579.1:c.*1320-26T>G	ENSP00000506867.1:n.*1320-26T>G
ENST00000683587.1:n.1927T>G
ENST00000683681.1:c.*100-26T>G	ENSP00000508110.1:n.*100-26T>G
ENST00000683735.1:c.*1794T>G	ENSP00000508336.1:n.*1794T>G
ENST00000683853.1:c.*227-26T>G	ENSP00000506834.1:n.*227-26T>G
ENST00000683860.1:c.*516T>G	ENSP00000507179.1:n.*516T>G
ENST00000683884.1:c.*723T>G	ENSP00000507004.1:n.*723T>G
ENST00000684041.1:c.*555-26T>G	ENSP00000508382.1:n.*555-26T>G
ENST00000684125.1:c.*82-26T>G	ENSP00000507320.1:n.*82-26T>G
ENST00000684203.1:n.3845T>G
ENST00000684231.1:c.*832-26T>G	ENSP00000507748.1:n.*832-26T>G
ENST00000684263.1:c.*1020T>G	ENSP00000508369.1:n.*1020T>G
ENST00000684305.1:c.1870-26T>G	ENSP00000506819.1:n.1870-26T>G
ENST00000684415.1:c.*947T>G	ENSP00000507227.1:n.*947T>G
ENST00000684520.1:c.*655T>G	ENSP00000506826.1:n.*655T>G
ENST00000684602.1:c.*1088-26T>G	ENSP00000507996.1:n.*1088-26T>G
ENST00000684667.1:c.1753-26T>G	ENSP00000507003.1:n.1753-26T>G
ENST00000268097.10:c.1422-26T>G MANE Select	ENSP00000268097.6:n.1422-26T>G
ENST00000268097.9:c.1422-26T>G	ENSP00000268097.5:n.1422-26T>G
ENST00000379915.4:c.504-26T>G	ENSP00000478716.1:n.504-26T>G
ENST00000564677.5:n.214-26T>G
ENST00000565873.1:n.307T>G
ENST00000566304.5:c.1455-26T>G	ENSP00000455114.1:n.1455-26T>G
ENST00000567027.5:c.1037-26T>G
ENST00000567159.5:c.1422-26T>G	ENSP00000456489.1:n.1422-26T>G
ENST00000567411.5:c.*943-26T>G	ENSP00000455545.1:n.*943-26T>G
ENST00000568777.5:n.6642-26T>G
ENST00000569116.1:n.129-26T>G
NM_000520.4:c.1422-26T>G	NP_000511.2:n.1422-26T>G
NM_000520.5:c.1422-26T>G	NP_000511.2:n.1422-26T>G
NM_001318825.1:c.1455-26T>G	NP_001305754.1:n.1455-26T>G
NR_134869.1:n.1666-26T>G
NM_000520.6:c.1422-26T>G MANE Select	NP_000511.2:n.1422-26T>G
NM_001318825.2:c.1455-26T>G	NP_001305754.1:n.1455-26T>G
NR_134869.2:n.1207-26T>G
NR_134869.3:n.1207-26T>G