Canonical Allele Identifier: CA342725596

Gene: GBA1

Linked Data

• MyVariant Identifiers: chr1:g.155209419A>G (hg19) ; chr1:g.155239628A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155239628A>G , CM000663.2:g.155239628A>G	GRCh38
NC_000001.10:g.155209419A>G , CM000663.1:g.155209419A>G	GRCh37
NC_000001.9:g.153476043A>G	NCBI36
NG_009783.1:g.10070T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.442T>C MANE Select	ENSP00000357357.3:p.Phe148Leu
ENST00000327247.9:c.442T>C	ENSP00000314508.5:p.Phe148Leu
ENST00000368373.7:c.442T>C	ENSP00000357357.3:p.Phe148Leu
ENST00000427500.7:c.307+258T>C	ENSP00000402577.2:n.307+258T>C
ENST00000428024.3:c.181T>C	ENSP00000397986.2:p.Phe61Leu
ENST00000473570.5:n.763T>C
ENST00000484489.5:n.339+345T>C
ENST00000493842.5:n.780T>C
ENST00000497670.5:n.77+258T>C
NM_000157.3:c.442T>C	NP_000148.2:p.Phe148Leu
NM_001005741.2:c.442T>C	NP_001005741.1:p.Phe148Leu
NM_001005742.2:c.442T>C	NP_001005742.1:p.Phe148Leu
NM_001171811.1:c.181T>C	NP_001165282.1:p.Phe61Leu
NM_001171812.1:c.307+258T>C	NP_001165283.1:n.307+258T>C
XM_006711270.1:c.442T>C	XP_006711333.1:p.Phe148Leu
XM_011509407.1:c.442T>C	XP_011507709.1:p.Phe148Leu
NM_000157.4:c.442T>C MANE Select	NP_000148.2:p.Phe148Leu
NM_001005741.3:c.442T>C	NP_001005741.1:p.Phe148Leu
NM_001005742.3:c.442T>C	NP_001005742.1:p.Phe148Leu
NM_001171811.2:c.181T>C	NP_001165282.1:p.Phe61Leu
NM_001171812.2:c.307+258T>C	NP_001165283.1:n.307+258T>C