Canonical Allele Identifier: CA2186742348
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72343451T= , CM000677.2:g.72343451T= GRCh38
NC_000015.9:g.72635792T= , CM000677.1:g.72635792T= GRCh37
NC_000015.8:g.70422846T= NCBI36
NG_009017.1:g.37729A=
NG_009017.2:g.37729A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000683243.1:c.*1369A= ENSP00000507042.1:n.*1369A=
ENST00000684263.1:c.*1840A= ENSP00000508369.1:n.*1840A=
ENST00000268097.10:c.*626A= MANE Select ENSP00000268097.6:n.*626A=
ENST00000268097.9:c.*626A= ENSP00000268097.5:n.*626A=
ENST00000379915.4:c.608+1995A= ENSP00000478716.1:n.608+1995A=
NM_000520.4:c.*626A= NP_000511.2:n.*626A=
NM_000520.5:c.*626A= NP_000511.2:n.*626A=
NM_001318825.1:c.*626A= NP_001305754.1:n.*626A=
NM_000520.6:c.*626A= MANE Select NP_000511.2:n.*626A=
NM_001318825.2:c.*626A= NP_001305754.1:n.*626A=