Canonical Allele Identifier: CA5050400

Gene: GBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35739782G>A , CM000671.2:g.35739782G>A	GRCh38
NC_000009.11:g.35739779G>A , CM000671.1:g.35739779G>A	GRCh37
NC_000009.10:g.35729779G>A	NCBI36
NG_033899.1:g.14447C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020944.3:c.1428C>T MANE Select	NP_065995.1:p.Tyr476=
ENST00000378103.7:c.1428C>T MANE Select	ENSP00000367343.3:p.Tyr476=
NM_001330660.1:c.1428C>T	NP_001317589.1:p.Tyr476=
NM_001330660.2:c.1428C>T	NP_001317589.1:p.Tyr476=
NM_020944.2:c.1428C>T	NP_065995.1:p.Tyr476=
ENST00000378094.4:c.1428C>T	ENSP00000367334.4:p.Tyr476=
ENST00000467252.5:n.1000C>T
XM_005251526.3:c.1446C>T	XP_005251583.1:p.Tyr482=
XM_005251526.5:c.1446C>T	XP_005251583.1:p.Tyr482=
XM_006716809.2:c.1446C>T	XP_006716872.1:p.Tyr482=
XM_006716809.4:c.1446C>T	XP_006716872.1:p.Tyr482=
XM_011517969.1:c.1446C>T	XP_011516271.1:p.Tyr482=
XM_011517970.1:c.1428C>T	XP_011516272.1:p.Tyr476=
XM_011517971.1:c.1446C>T	XP_011516273.1:p.Tyr482=
XM_011517972.1:c.1446C>T	XP_011516274.1:p.Tyr482=
XM_011517973.1:c.1428C>T	XP_011516275.1:p.Tyr476=
XM_011517974.1:c.1209C>T	XP_011516276.1:p.Tyr403=
XM_011517975.1:c.993C>T	XP_011516277.1:p.Tyr331=
XM_011517976.1:c.975C>T	XP_011516278.1:p.Tyr325=
XM_011517977.1:c.891C>T	XP_011516279.1:p.Tyr297=
XM_011517978.1:c.873C>T	XP_011516280.1:p.Tyr291=
XM_011517979.1:c.873C>T	XP_011516281.1:p.Tyr291=
XM_017014937.2:c.1428C>T	XP_016870426.1:p.Tyr476=
XM_017014938.2:c.1446C>T	XP_016870427.1:p.Tyr482=
XM_017014939.2:c.1428C>T	XP_016870428.1:p.Tyr476=
XM_017014940.2:c.1209C>T	XP_016870429.1:p.Tyr403=
XM_017014941.2:c.1209C>T	XP_016870430.1:p.Tyr403=
XM_017014942.2:c.993C>T	XP_016870431.1:p.Tyr331=
XM_017014943.2:c.975C>T	XP_016870432.1:p.Tyr325=
XM_017014944.1:c.891C>T	XP_016870433.1:p.Tyr297=
XM_017014945.1:c.873C>T	XP_016870434.1:p.Tyr291=
XM_017014946.2:c.567C>T	XP_016870435.1:p.Tyr189=