Canonical Allele Identifier: CA342727124

Gene: GBA1

Linked Data

• MyVariant Identifiers: chr1:g.155209721A>G (hg19) ; chr1:g.155239930A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155239930A>G , CM000663.2:g.155239930A>G	GRCh38
NC_000001.10:g.155209721A>G , CM000663.1:g.155209721A>G	GRCh37
NC_000001.9:g.153476345A>G	NCBI36
NG_009783.1:g.9768T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.263T>C MANE Select	ENSP00000357357.3:p.Met88Thr
ENST00000327247.9:c.263T>C	ENSP00000314508.5:p.Met88Thr
ENST00000368373.7:c.263T>C	ENSP00000357357.3:p.Met88Thr
ENST00000427500.7:c.263T>C	ENSP00000402577.2:p.Met88Thr
ENST00000428024.3:c.2T>C	ENSP00000397986.2:p.Met1Thr
ENST00000467918.5:n.453T>C
ENST00000473570.5:n.584T>C
ENST00000484489.5:n.339+43T>C
ENST00000493842.5:n.601T>C
ENST00000497670.5:n.33T>C
NM_000157.3:c.263T>C	NP_000148.2:p.Met88Thr
NM_001005741.2:c.263T>C	NP_001005741.1:p.Met88Thr
NM_001005742.2:c.263T>C	NP_001005742.1:p.Met88Thr
NM_001171811.1:c.2T>C	NP_001165282.1:p.Met1Thr
NM_001171812.1:c.263T>C	NP_001165283.1:p.Met88Thr
XM_006711270.1:c.263T>C	XP_006711333.1:p.Met88Thr
XM_011509407.1:c.263T>C	XP_011507709.1:p.Met88Thr
NM_000157.4:c.263T>C MANE Select	NP_000148.2:p.Met88Thr
NM_001005741.3:c.263T>C	NP_001005741.1:p.Met88Thr
NM_001005742.3:c.263T>C	NP_001005742.1:p.Met88Thr
NM_001171811.2:c.2T>C	NP_001165282.1:p.Met1Thr
NM_001171812.2:c.263T>C	NP_001165283.1:p.Met88Thr