Canonical Allele Identifier: CA5050436

Gene: GBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35740050C>T , CM000671.2:g.35740050C>T	GRCh38
NC_000009.11:g.35740047C>T , CM000671.1:g.35740047C>T	GRCh37
NC_000009.10:g.35730047C>T	NCBI36
NG_033899.1:g.14179G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020944.3:c.1357G>A MANE Select	NP_065995.1:p.Ala453Thr
ENST00000378103.7:c.1357G>A MANE Select	ENSP00000367343.3:p.Ala453Thr
NM_001330660.1:c.1357G>A	NP_001317589.1:p.Ala453Thr
NM_001330660.2:c.1357G>A	NP_001317589.1:p.Ala453Thr
NM_020944.2:c.1357G>A	NP_065995.1:p.Ala453Thr
ENST00000378094.4:c.1357G>A	ENSP00000367334.4:p.Ala453Thr
ENST00000467252.5:n.929G>A
XM_005251526.3:c.1375G>A	XP_005251583.1:p.Ala459Thr
XM_005251526.5:c.1375G>A	XP_005251583.1:p.Ala459Thr
XM_006716809.2:c.1375G>A	XP_006716872.1:p.Ala459Thr
XM_006716809.4:c.1375G>A	XP_006716872.1:p.Ala459Thr
XM_011517969.1:c.1375G>A	XP_011516271.1:p.Ala459Thr
XM_011517970.1:c.1357G>A	XP_011516272.1:p.Ala453Thr
XM_011517971.1:c.1375G>A	XP_011516273.1:p.Ala459Thr
XM_011517972.1:c.1375G>A	XP_011516274.1:p.Ala459Thr
XM_011517973.1:c.1357G>A	XP_011516275.1:p.Ala453Thr
XM_011517974.1:c.1138G>A	XP_011516276.1:p.Ala380Thr
XM_011517975.1:c.922G>A	XP_011516277.1:p.Ala308Thr
XM_011517976.1:c.904G>A	XP_011516278.1:p.Ala302Thr
XM_011517977.1:c.820G>A	XP_011516279.1:p.Ala274Thr
XM_011517978.1:c.802G>A	XP_011516280.1:p.Ala268Thr
XM_011517979.1:c.802G>A	XP_011516281.1:p.Ala268Thr
XM_017014937.2:c.1357G>A	XP_016870426.1:p.Ala453Thr
XM_017014938.2:c.1375G>A	XP_016870427.1:p.Ala459Thr
XM_017014939.2:c.1357G>A	XP_016870428.1:p.Ala453Thr
XM_017014940.2:c.1138G>A	XP_016870429.1:p.Ala380Thr
XM_017014941.2:c.1138G>A	XP_016870430.1:p.Ala380Thr
XM_017014942.2:c.922G>A	XP_016870431.1:p.Ala308Thr
XM_017014943.2:c.904G>A	XP_016870432.1:p.Ala302Thr
XM_017014944.1:c.820G>A	XP_016870433.1:p.Ala274Thr
XM_017014945.1:c.802G>A	XP_016870434.1:p.Ala268Thr
XM_017014946.2:c.496G>A	XP_016870435.1:p.Ala166Thr