Canonical Allele Identifier: CA491112381

Gene: HEXA

Linked Data

• gnomAD v4: 15-72345649-C-A
• MyVariant Identifiers: chr15:g.72637990C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72345649C>A , CM000677.2:g.72345649C>A	GRCh38
NC_000015.9:g.72637990C>A , CM000677.1:g.72637990C>A	GRCh37
NC_000015.8:g.70425044C>A	NCBI36
NG_009017.1:g.35531G>T
NG_009017.2:g.35531G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.*82-99G>T	ENSP00000457521.2:n.*82-99G>T
ENST00000682061.1:c.*1669G>T	ENSP00000508316.1:n.*1669G>T
ENST00000682064.1:n.1550G>T
ENST00000682177.1:c.1465-99G>T	ENSP00000507409.1:n.1465-99G>T
ENST00000682235.1:n.1346G>T
ENST00000682461.1:c.1528-99G>T	ENSP00000507308.1:n.1528-99G>T
ENST00000682653.1:n.2327G>T
ENST00000682657.1:c.*1160G>T	ENSP00000507753.1:n.*1160G>T
ENST00000682721.1:c.*1225-99G>T	ENSP00000507535.1:n.*1225-99G>T
ENST00000682843.1:c.*1063-99G>T	ENSP00000508173.1:n.*1063-99G>T
ENST00000683003.1:c.*1160G>T	ENSP00000507576.1:n.*1160G>T
ENST00000683133.1:c.1606-99G>T	ENSP00000508108.1:n.1606-99G>T
ENST00000683243.1:c.*575-99G>T	ENSP00000507042.1:n.*575-99G>T
ENST00000683463.1:c.*812G>T	ENSP00000507986.1:n.*812G>T
ENST00000683548.1:n.1781G>T
ENST00000683579.1:c.*1320-99G>T	ENSP00000506867.1:n.*1320-99G>T
ENST00000683587.1:n.1854G>T
ENST00000683681.1:c.*99+28G>T	ENSP00000508110.1:n.*99+28G>T
ENST00000683735.1:c.*1721G>T	ENSP00000508336.1:n.*1721G>T
ENST00000683853.1:c.*227-99G>T	ENSP00000506834.1:n.*227-99G>T
ENST00000683860.1:c.*443G>T	ENSP00000507179.1:n.*443G>T
ENST00000683884.1:c.*650G>T	ENSP00000507004.1:n.*650G>T
ENST00000684041.1:c.*554+28G>T	ENSP00000508382.1:n.*554+28G>T
ENST00000684125.1:c.*82-99G>T	ENSP00000507320.1:n.*82-99G>T
ENST00000684203.1:n.3772G>T
ENST00000684231.1:c.*832-99G>T	ENSP00000507748.1:n.*832-99G>T
ENST00000684263.1:c.*947G>T	ENSP00000508369.1:n.*947G>T
ENST00000684305.1:c.1870-99G>T	ENSP00000506819.1:n.1870-99G>T
ENST00000684415.1:c.*874G>T	ENSP00000507227.1:n.*874G>T
ENST00000684520.1:c.*582G>T	ENSP00000506826.1:n.*582G>T
ENST00000684602.1:c.*1088-99G>T	ENSP00000507996.1:n.*1088-99G>T
ENST00000684667.1:c.1753-99G>T	ENSP00000507003.1:n.1753-99G>T
ENST00000268097.10:c.1422-99G>T MANE Select	ENSP00000268097.6:n.1422-99G>T
ENST00000268097.9:c.1422-99G>T	ENSP00000268097.5:n.1422-99G>T
ENST00000379915.4:c.504-99G>T	ENSP00000478716.1:n.504-99G>T
ENST00000564677.5:n.213+28G>T
ENST00000565873.1:n.234G>T
ENST00000566304.5:c.1455-99G>T	ENSP00000455114.1:n.1455-99G>T
ENST00000567027.5:c.1037-99G>T
ENST00000567159.5:c.1422-99G>T	ENSP00000456489.1:n.1422-99G>T
ENST00000567411.5:c.*943-99G>T	ENSP00000455545.1:n.*943-99G>T
ENST00000568777.5:n.6642-99G>T
ENST00000569116.1:n.128+28G>T
NM_000520.4:c.1422-99G>T	NP_000511.2:n.1422-99G>T
NM_000520.5:c.1422-99G>T	NP_000511.2:n.1422-99G>T
NM_001318825.1:c.1455-99G>T	NP_001305754.1:n.1455-99G>T
NR_134869.1:n.1666-99G>T
NM_000520.6:c.1422-99G>T MANE Select	NP_000511.2:n.1422-99G>T
NM_001318825.2:c.1455-99G>T	NP_001305754.1:n.1455-99G>T
NR_134869.2:n.1207-99G>T
NR_134869.3:n.1207-99G>T