Canonical Allele Identifier: CA5050760
Community Standard Title: NM_020944.3(GBA2):c.326G>A (p.Ser109Asn)
Gene: GBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35748379C>T , CM000671.2:g.35748379C>T GRCh38
NC_000009.11:g.35748376C>T , CM000671.1:g.35748376C>T GRCh37
NC_000009.10:g.35738376C>T NCBI36
NG_033899.1:g.5850G>A

Transcript Alleles

HGVS Amino-acid Change
NM_020944.3:c.326G>A MANE Select NP_065995.1:p.Ser109Asn
ENST00000378103.7:c.326G>A MANE Select ENSP00000367343.3:p.Ser109Asn
NM_001330660.1:c.326G>A NP_001317589.1:p.Ser109Asn
NM_001330660.2:c.326G>A NP_001317589.1:p.Ser109Asn
NM_020944.2:c.326G>A NP_065995.1:p.Ser109Asn
ENST00000378094.4:c.326G>A ENSP00000367334.4:p.Ser109Asn
ENST00000489025.1:n.595G>A
XM_005251526.3:c.326G>A XP_005251583.1:p.Ser109Asn
XM_005251526.5:c.326G>A XP_005251583.1:p.Ser109Asn
XM_006716809.2:c.326G>A XP_006716872.1:p.Ser109Asn
XM_006716809.4:c.326G>A XP_006716872.1:p.Ser109Asn
XM_011517969.1:c.326G>A XP_011516271.1:p.Ser109Asn
XM_011517970.1:c.326G>A XP_011516272.1:p.Ser109Asn
XM_011517971.1:c.326G>A XP_011516273.1:p.Ser109Asn
XM_011517972.1:c.326G>A XP_011516274.1:p.Ser109Asn
XM_011517973.1:c.326G>A XP_011516275.1:p.Ser109Asn
XM_011517974.1:c.326G>A XP_011516276.1:p.Ser109Asn
XM_011517975.1:c.-123G>A XP_011516277.1:n.-123G>A
XM_011517976.1:c.-123G>A XP_011516278.1:n.-123G>A
XM_017014937.2:c.326G>A XP_016870426.1:p.Ser109Asn
XM_017014938.2:c.326G>A XP_016870427.1:p.Ser109Asn
XM_017014939.2:c.326G>A XP_016870428.1:p.Ser109Asn
XM_017014940.2:c.326G>A XP_016870429.1:p.Ser109Asn
XM_017014941.2:c.326G>A XP_016870430.1:p.Ser109Asn
XM_017014942.2:c.-123G>A XP_016870431.1:n.-123G>A
XM_017014943.2:c.-123G>A XP_016870432.1:n.-123G>A
XM_017014946.2:c.-587G>A XP_016870435.1:n.-587G>A