Canonical Allele Identifier: CA491113993
Gene: HEXA HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.72638214C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345873C>T , CM000677.2:g.72345873C>T GRCh38
NC_000015.9:g.72638214C>T , CM000677.1:g.72638214C>T GRCh37
NC_000015.8:g.70425268C>T NCBI36
NG_009017.1:g.35307G>A
NG_009017.2:g.35307G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*82-323G>A ENSP00000457521.2:n.*82-323G>A
ENST00000682061.1:c.*1445G>A ENSP00000508316.1:n.*1445G>A
ENST00000682064.1:n.1326G>A
ENST00000682177.1:c.1465-323G>A ENSP00000507409.1:n.1465-323G>A
ENST00000682235.1:n.1122G>A
ENST00000682461.1:c.1528-323G>A ENSP00000507308.1:n.1528-323G>A
ENST00000682653.1:n.2103G>A
ENST00000682657.1:c.*936G>A ENSP00000507753.1:n.*936G>A
ENST00000682721.1:c.*1225-323G>A ENSP00000507535.1:n.*1225-323G>A
ENST00000682843.1:c.*1063-323G>A ENSP00000508173.1:n.*1063-323G>A
ENST00000683003.1:c.*936G>A ENSP00000507576.1:n.*936G>A
ENST00000683133.1:c.1606-323G>A ENSP00000508108.1:n.1606-323G>A
ENST00000683243.1:c.*575-323G>A ENSP00000507042.1:n.*575-323G>A
ENST00000683463.1:c.*588G>A ENSP00000507986.1:n.*588G>A
ENST00000683548.1:n.1557G>A
ENST00000683579.1:c.*1320-323G>A ENSP00000506867.1:n.*1320-323G>A
ENST00000683587.1:n.1630G>A
ENST00000683681.1:c.1422-97G>A ENSP00000508110.1:n.1422-97G>A
ENST00000683735.1:c.*1497G>A ENSP00000508336.1:n.*1497G>A
ENST00000683853.1:c.*227-323G>A ENSP00000506834.1:n.*227-323G>A
ENST00000683860.1:c.*219G>A ENSP00000507179.1:n.*219G>A
ENST00000683884.1:c.*426G>A ENSP00000507004.1:n.*426G>A
ENST00000684041.1:c.*358G>A ENSP00000508382.1:n.*358G>A
ENST00000684125.1:c.*82-323G>A ENSP00000507320.1:n.*82-323G>A
ENST00000684203.1:n.3548G>A
ENST00000684231.1:c.*832-323G>A ENSP00000507748.1:n.*832-323G>A
ENST00000684263.1:c.*723G>A ENSP00000508369.1:n.*723G>A
ENST00000684305.1:c.1870-323G>A ENSP00000506819.1:n.1870-323G>A
ENST00000684415.1:c.*650G>A ENSP00000507227.1:n.*650G>A
ENST00000684520.1:c.*358G>A ENSP00000506826.1:n.*358G>A
ENST00000684602.1:c.*1088-323G>A ENSP00000507996.1:n.*1088-323G>A
ENST00000684667.1:c.1753-323G>A ENSP00000507003.1:n.1753-323G>A
ENST00000268097.10:c.1422-323G>A MANE Select ENSP00000268097.6:n.1422-323G>A
ENST00000268097.9:c.1422-323G>A ENSP00000268097.5:n.1422-323G>A
ENST00000379915.4:c.504-323G>A ENSP00000478716.1:n.504-323G>A
ENST00000564677.5:n.17G>A
ENST00000565873.1:n.10G>A
ENST00000566304.5:c.1455-323G>A ENSP00000455114.1:n.1455-323G>A
ENST00000567027.5:c.1037-323G>A
ENST00000567159.5:c.1422-323G>A ENSP00000456489.1:n.1422-323G>A
ENST00000567411.5:c.*943-323G>A ENSP00000455545.1:n.*943-323G>A
ENST00000568777.5:n.6642-323G>A
NM_000520.4:c.1422-323G>A NP_000511.2:n.1422-323G>A
NM_000520.5:c.1422-323G>A NP_000511.2:n.1422-323G>A
NM_001318825.1:c.1455-323G>A NP_001305754.1:n.1455-323G>A
NR_134869.1:n.1666-323G>A
NM_000520.6:c.1422-323G>A MANE Select NP_000511.2:n.1422-323G>A
NM_001318825.2:c.1455-323G>A NP_001305754.1:n.1455-323G>A
NR_134869.2:n.1207-323G>A
NR_134869.3:n.1207-323G>A