Canonical Allele Identifier: CA491475536
Gene: HEXA HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.72668200G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72375859G>C , CM000677.2:g.72375859G>C GRCh38
NC_000015.9:g.72668200G>C , CM000677.1:g.72668200G>C GRCh37
NC_000015.8:g.70455254G>C NCBI36
NG_009017.1:g.5321C>G
NG_009017.2:g.5321C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000268097.10:c.114C>G MANE Select ENSP00000268097.6:p.Val38=
ENST00000268097.9:c.114C>G ENSP00000268097.5:p.Val38=
ENST00000379915.4:c.114C>G ENSP00000478716.1:p.Val38=
ENST00000563762.5:n.114C>G ENSP00000456346.1:p.Val38=
ENST00000563908.1:n.111C>G
ENST00000566304.5:c.114C>G ENSP00000455114.1:p.Val38=
ENST00000566672.5:c.114C>G ENSP00000457037.1:p.Val38=
ENST00000567159.5:c.114C>G ENSP00000456489.1:p.Val38=
ENST00000567213.2:c.114C>G ENSP00000478217.1:p.Val38=
ENST00000567411.5:c.114C>G ENSP00000455545.1:p.Val38=
ENST00000568260.1:n.95C>G
ENST00000569410.5:c.114C>G ENSP00000457125.1:p.Val38=
ENST00000569509.5:n.147-28C>G
NM_000520.4:c.114C>G NP_000511.2:p.Val38=
NM_000520.5:c.114C>G NP_000511.2:p.Val38=
NM_001318825.1:c.114C>G NP_001305754.1:p.Val38=
NR_134869.1:n.615C>G
NM_000520.6:c.114C>G MANE Select NP_000511.2:p.Val38=
NM_001318825.2:c.114C>G NP_001305754.1:p.Val38=
NR_134869.2:n.156C>G
NR_134869.3:n.156C>G