Canonical Allele Identifier: CA491111791

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72637895G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72345554G>C , CM000677.2:g.72345554G>C	GRCh38
NC_000015.9:g.72637895G>C , CM000677.1:g.72637895G>C	GRCh37
NC_000015.8:g.70424949G>C	NCBI36
NG_009017.1:g.35626C>G
NG_009017.2:g.35626C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.*82-4C>G	ENSP00000457521.2:n.*82-4C>G
ENST00000682061.1:c.*1764C>G	ENSP00000508316.1:n.*1764C>G
ENST00000682064.1:n.1645C>G
ENST00000682177.1:c.1465-4C>G	ENSP00000507409.1:n.1465-4C>G
ENST00000682235.1:n.1441C>G
ENST00000682461.1:c.1528-4C>G	ENSP00000507308.1:n.1528-4C>G
ENST00000682653.1:n.2422C>G
ENST00000682657.1:c.*1255C>G	ENSP00000507753.1:n.*1255C>G
ENST00000682721.1:c.*1225-4C>G	ENSP00000507535.1:n.*1225-4C>G
ENST00000682843.1:c.*1063-4C>G	ENSP00000508173.1:n.*1063-4C>G
ENST00000683003.1:c.*1255C>G	ENSP00000507576.1:n.*1255C>G
ENST00000683133.1:c.1606-4C>G	ENSP00000508108.1:n.1606-4C>G
ENST00000683243.1:c.*575-4C>G	ENSP00000507042.1:n.*575-4C>G
ENST00000683463.1:c.*907C>G	ENSP00000507986.1:n.*907C>G
ENST00000683548.1:n.1876C>G
ENST00000683579.1:c.*1320-4C>G	ENSP00000506867.1:n.*1320-4C>G
ENST00000683587.1:n.1949C>G
ENST00000683681.1:c.*100-4C>G	ENSP00000508110.1:n.*100-4C>G
ENST00000683735.1:c.*1816C>G	ENSP00000508336.1:n.*1816C>G
ENST00000683853.1:c.*227-4C>G	ENSP00000506834.1:n.*227-4C>G
ENST00000683860.1:c.*538C>G	ENSP00000507179.1:n.*538C>G
ENST00000683884.1:c.*745C>G	ENSP00000507004.1:n.*745C>G
ENST00000684041.1:c.*555-4C>G	ENSP00000508382.1:n.*555-4C>G
ENST00000684125.1:c.*82-4C>G	ENSP00000507320.1:n.*82-4C>G
ENST00000684203.1:n.3867C>G
ENST00000684231.1:c.*832-4C>G	ENSP00000507748.1:n.*832-4C>G
ENST00000684263.1:c.*1042C>G	ENSP00000508369.1:n.*1042C>G
ENST00000684305.1:c.1870-4C>G	ENSP00000506819.1:n.1870-4C>G
ENST00000684415.1:c.*969C>G	ENSP00000507227.1:n.*969C>G
ENST00000684520.1:c.*677C>G	ENSP00000506826.1:n.*677C>G
ENST00000684602.1:c.*1088-4C>G	ENSP00000507996.1:n.*1088-4C>G
ENST00000684667.1:c.1753-4C>G	ENSP00000507003.1:n.1753-4C>G
ENST00000268097.10:c.1422-4C>G MANE Select	ENSP00000268097.6:n.1422-4C>G
ENST00000268097.9:c.1422-4C>G	ENSP00000268097.5:n.1422-4C>G
ENST00000379915.4:c.504-4C>G	ENSP00000478716.1:n.504-4C>G
ENST00000564677.5:n.214-4C>G
ENST00000565873.1:n.329C>G
ENST00000566304.5:c.1455-4C>G	ENSP00000455114.1:n.1455-4C>G
ENST00000567027.5:c.1037-4C>G
ENST00000567159.5:c.1422-4C>G	ENSP00000456489.1:n.1422-4C>G
ENST00000567411.5:c.*943-4C>G	ENSP00000455545.1:n.*943-4C>G
ENST00000568777.5:n.6642-4C>G
ENST00000569116.1:n.129-4C>G
NM_000520.4:c.1422-4C>G	NP_000511.2:n.1422-4C>G
NM_000520.5:c.1422-4C>G	NP_000511.2:n.1422-4C>G
NM_001318825.1:c.1455-4C>G	NP_001305754.1:n.1455-4C>G
NR_134869.1:n.1666-4C>G
NM_000520.6:c.1422-4C>G MANE Select	NP_000511.2:n.1422-4C>G
NM_001318825.2:c.1455-4C>G	NP_001305754.1:n.1455-4C>G
NR_134869.2:n.1207-4C>G
NR_134869.3:n.1207-4C>G