Canonical Allele Identifier: CA5050572

Gene: GBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35740887G>A , CM000671.2:g.35740887G>A	GRCh38
NC_000009.11:g.35740884G>A , CM000671.1:g.35740884G>A	GRCh37
NC_000009.10:g.35730884G>A	NCBI36
NG_033899.1:g.13342C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020944.3:c.964C>T MANE Select	NP_065995.1:p.Leu322=
ENST00000378103.7:c.964C>T MANE Select	ENSP00000367343.3:p.Leu322=
NM_001330660.1:c.964C>T	NP_001317589.1:p.Leu322=
NM_001330660.2:c.964C>T	NP_001317589.1:p.Leu322=
NM_020944.2:c.964C>T	NP_065995.1:p.Leu322=
ENST00000378094.4:c.964C>T	ENSP00000367334.4:p.Leu322=
ENST00000467252.5:n.536C>T
XM_005251526.3:c.982C>T	XP_005251583.1:p.Leu328=
XM_005251526.5:c.982C>T	XP_005251583.1:p.Leu328=
XM_006716809.2:c.982C>T	XP_006716872.1:p.Leu328=
XM_006716809.4:c.982C>T	XP_006716872.1:p.Leu328=
XM_011517969.1:c.982C>T	XP_011516271.1:p.Leu328=
XM_011517970.1:c.964C>T	XP_011516272.1:p.Leu322=
XM_011517971.1:c.982C>T	XP_011516273.1:p.Leu328=
XM_011517972.1:c.982C>T	XP_011516274.1:p.Leu328=
XM_011517973.1:c.964C>T	XP_011516275.1:p.Leu322=
XM_011517974.1:c.745C>T	XP_011516276.1:p.Leu249=
XM_011517975.1:c.529C>T	XP_011516277.1:p.Leu177=
XM_011517976.1:c.511C>T	XP_011516278.1:p.Leu171=
XM_011517977.1:c.427C>T	XP_011516279.1:p.Leu143=
XM_011517978.1:c.409C>T	XP_011516280.1:p.Leu137=
XM_011517979.1:c.409C>T	XP_011516281.1:p.Leu137=
XM_017014937.2:c.964C>T	XP_016870426.1:p.Leu322=
XM_017014938.2:c.982C>T	XP_016870427.1:p.Leu328=
XM_017014939.2:c.964C>T	XP_016870428.1:p.Leu322=
XM_017014940.2:c.745C>T	XP_016870429.1:p.Leu249=
XM_017014941.2:c.745C>T	XP_016870430.1:p.Leu249=
XM_017014942.2:c.529C>T	XP_016870431.1:p.Leu177=
XM_017014943.2:c.511C>T	XP_016870432.1:p.Leu171=
XM_017014944.1:c.427C>T	XP_016870433.1:p.Leu143=
XM_017014945.1:c.409C>T	XP_016870434.1:p.Leu137=
XM_017014946.2:c.103C>T	XP_016870435.1:p.Leu35=