Canonical Allele Identifier: CA2481201913
Gene: GBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155236200A= , CM000663.2:g.155236200A= GRCh38
NC_000001.10:g.155205991A= , CM000663.1:g.155205991A= GRCh37
NC_000001.9:g.153472615A= NCBI36
NG_009783.1:g.13498T=

Transcript Alleles

HGVS Amino-acid change
ENST00000368373.8:c.1224+45T= MANE Select ENSP00000357357.3:n.1224+45T=
ENST00000327247.9:c.1224+45T= ENSP00000314508.5:n.1224+45T=
ENST00000368373.7:c.1224+45T= ENSP00000357357.3:n.1224+45T=
ENST00000427500.7:c.1077+45T= ENSP00000402577.2:n.1077+45T=
ENST00000428024.3:c.963+45T= ENSP00000397986.2:n.963+45T=
ENST00000478472.1:n.215+45T=
ENST00000484489.5:n.383+45T=
ENST00000491081.5:n.874T=
NM_000157.3:c.1224+45T= NP_000148.2:n.1224+45T=
NM_001005741.2:c.1224+45T= NP_001005741.1:n.1224+45T=
NM_001005742.2:c.1224+45T= NP_001005742.1:n.1224+45T=
NM_001171811.1:c.963+45T= NP_001165282.1:n.963+45T=
NM_001171812.1:c.1077+45T= NP_001165283.1:n.1077+45T=
XM_006711270.1:c.1224+45T= XP_006711333.1:n.1224+45T=
XM_011509407.1:c.1224+45T= XP_011507709.1:n.1224+45T=
NM_000157.4:c.1224+45T= MANE Select NP_000148.2:n.1224+45T=
NM_001005741.3:c.1224+45T= NP_001005741.1:n.1224+45T=
NM_001005742.3:c.1224+45T= NP_001005742.1:n.1224+45T=
NM_001171811.2:c.963+45T= NP_001165282.1:n.963+45T=
NM_001171812.2:c.1077+45T= NP_001165283.1:n.1077+45T=