Canonical Allele Identifier: CA393059203

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72638618C>A (hg19) ; chr15:g.72346277C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72346277C>A , CM000677.2:g.72346277C>A	GRCh38
NC_000015.9:g.72638618C>A , CM000677.1:g.72638618C>A	GRCh37
NC_000015.8:g.70425672C>A	NCBI36
NG_009017.1:g.34903G>T
NG_009017.2:g.34903G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.*39G>T	ENSP00000457521.2:n.*39G>T
ENST00000682061.1:c.*1041G>T	ENSP00000508316.1:n.*1041G>T
ENST00000682064.1:n.922G>T
ENST00000682177.1:c.1422G>T	ENSP00000507409.1:n.1422G>T
ENST00000682235.1:n.718G>T
ENST00000682461.1:c.1485G>T	ENSP00000507308.1:n.1485G>T
ENST00000682653.1:n.1699G>T
ENST00000682657.1:c.*532G>T	ENSP00000507753.1:n.*532G>T
ENST00000682721.1:c.*1182G>T	ENSP00000507535.1:n.*1182G>T
ENST00000682843.1:c.*1020G>T	ENSP00000508173.1:n.*1020G>T
ENST00000683003.1:c.*532G>T	ENSP00000507576.1:n.*532G>T
ENST00000683133.1:c.1563G>T	ENSP00000508108.1:n.1563G>T
ENST00000683243.1:c.*532G>T	ENSP00000507042.1:n.*532G>T
ENST00000683463.1:c.*184G>T	ENSP00000507986.1:n.*184G>T
ENST00000683548.1:n.1153G>T
ENST00000683579.1:c.*1277G>T	ENSP00000506867.1:n.*1277G>T
ENST00000683587.1:n.1226G>T
ENST00000683681.1:c.1379G>T	ENSP00000508110.1:p.Trp460Leu
ENST00000683735.1:c.*1093G>T	ENSP00000508336.1:n.*1093G>T
ENST00000683853.1:c.*184G>T	ENSP00000506834.1:n.*184G>T
ENST00000683860.1:c.1379G>T	ENSP00000507179.1:p.Trp460Leu
ENST00000683884.1:c.*22G>T	ENSP00000507004.1:n.*22G>T
ENST00000684041.1:c.1379G>T	ENSP00000508382.1:p.Trp460Leu
ENST00000684125.1:c.*39G>T	ENSP00000507320.1:n.*39G>T
ENST00000684203.1:n.3144G>T
ENST00000684231.1:c.*789G>T	ENSP00000507748.1:n.*789G>T
ENST00000684263.1:c.*319G>T	ENSP00000508369.1:n.*319G>T
ENST00000684305.1:c.1827G>T	ENSP00000506819.1:n.1827G>T
ENST00000684415.1:c.*246G>T	ENSP00000507227.1:n.*246G>T
ENST00000684520.1:c.1379G>T	ENSP00000506826.1:p.Trp460Leu
ENST00000684602.1:c.*1045G>T	ENSP00000507996.1:n.*1045G>T
ENST00000684667.1:c.1710G>T	ENSP00000507003.1:n.1710G>T
ENST00000268097.10:c.1379G>T MANE Select	ENSP00000268097.6:p.Trp460Leu
ENST00000268097.9:c.1379G>T	ENSP00000268097.5:p.Trp460Leu
ENST00000379915.4:c.461G>T	ENSP00000478716.1:p.Trp154Leu
ENST00000563762.5:c.874G>T	ENSP00000456346.1:n.874G>T
ENST00000566304.5:c.1412G>T	ENSP00000455114.1:p.Trp471Leu
ENST00000566672.5:c.*789G>T	ENSP00000457037.1:n.*789G>T
ENST00000567027.5:c.994G>T
ENST00000567159.5:c.1379G>T	ENSP00000456489.1:p.Trp460Leu
ENST00000567411.5:c.*900G>T	ENSP00000455545.1:n.*900G>T
ENST00000568777.5:n.6599G>T
ENST00000569410.5:c.*184G>T	ENSP00000457125.1:n.*184G>T
NM_000520.4:c.1379G>T	NP_000511.2:p.Trp460Leu
NM_000520.5:c.1379G>T	NP_000511.2:p.Trp460Leu
NM_001318825.1:c.1412G>T	NP_001305754.1:p.Trp471Leu
NR_134869.1:n.1623G>T
NM_000520.6:c.1379G>T MANE Select	NP_000511.2:p.Trp460Leu
NM_001318825.2:c.1412G>T	NP_001305754.1:p.Trp471Leu
NR_134869.2:n.1164G>T
NR_134869.3:n.1164G>T