Canonical Allele Identifier: CA421025601

Gene: GBA1

Linked Data

• MyVariant Identifiers: chr1:g.155207999C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238208C>A , CM000663.2:g.155238208C>A	GRCh38
NC_000001.10:g.155207999C>A , CM000663.1:g.155207999C>A	GRCh37
NC_000001.9:g.153474623C>A	NCBI36
NG_009783.1:g.11490G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.687G>T MANE Select	ENSP00000357357.3:p.Ala229=
ENST00000327247.9:c.687G>T	ENSP00000314508.5:p.Ala229=
ENST00000368373.7:c.687G>T	ENSP00000357357.3:p.Ala229=
ENST00000427500.7:c.540G>T	ENSP00000402577.2:p.Ala180=
ENST00000428024.3:c.426G>T	ENSP00000397986.2:p.Ala142=
ENST00000460156.1:n.474G>T
ENST00000484489.5:n.339+1765G>T
ENST00000491081.5:n.292G>T
ENST00000497670.5:n.310G>T
NM_000157.3:c.687G>T	NP_000148.2:p.Ala229=
NM_001005741.2:c.687G>T	NP_001005741.1:p.Ala229=
NM_001005742.2:c.687G>T	NP_001005742.1:p.Ala229=
NM_001171811.1:c.426G>T	NP_001165282.1:p.Ala142=
NM_001171812.1:c.540G>T	NP_001165283.1:p.Ala180=
XM_006711270.1:c.687G>T	XP_006711333.1:p.Ala229=
XM_011509407.1:c.687G>T	XP_011507709.1:p.Ala229=
NM_000157.4:c.687G>T MANE Select	NP_000148.2:p.Ala229=
NM_001005741.3:c.687G>T	NP_001005741.1:p.Ala229=
NM_001005742.3:c.687G>T	NP_001005742.1:p.Ala229=
NM_001171811.2:c.426G>T	NP_001165282.1:p.Ala142=
NM_001171812.2:c.540G>T	NP_001165283.1:p.Ala180=