Canonical Allele Identifier: CA421242965

Gene: GBA1

Linked Data

• MyVariant Identifiers: chr1:g.155205003A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155235212A>G , CM000663.2:g.155235212A>G	GRCh38
NC_000001.10:g.155205003A>G , CM000663.1:g.155205003A>G	GRCh37
NC_000001.9:g.153471627A>G	NCBI36
NG_009783.1:g.14486T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368373.8:c.1488T>C MANE Select	ENSP00000357357.3:p.Val496=
ENST00000327247.9:c.1488T>C	ENSP00000314508.5:p.Val496=
ENST00000368373.7:c.1488T>C	ENSP00000357357.3:p.Val496=
ENST00000427500.7:c.1341T>C	ENSP00000402577.2:p.Val447=
ENST00000428024.3:c.1227T>C	ENSP00000397986.2:p.Val409=
ENST00000464536.1:n.191-391T>C
ENST00000478472.1:n.848T>C
ENST00000484489.5:n.647T>C
NM_000157.3:c.1488T>C	NP_000148.2:p.Val496=
NM_001005741.2:c.1488T>C	NP_001005741.1:p.Val496=
NM_001005742.2:c.1488T>C	NP_001005742.1:p.Val496=
NM_001171811.1:c.1227T>C	NP_001165282.1:p.Val409=
NM_001171812.1:c.1341T>C	NP_001165283.1:p.Val447=
XM_006711270.1:c.1488T>C	XP_006711333.1:p.Val496=
XM_011509407.1:c.1488T>C	XP_011507709.1:p.Val496=
NM_000157.4:c.1488T>C MANE Select	NP_000148.2:p.Val496=
NM_001005741.3:c.1488T>C	NP_001005741.1:p.Val496=
NM_001005742.3:c.1488T>C	NP_001005742.1:p.Val496=
NM_001171811.2:c.1227T>C	NP_001165282.1:p.Val409=
NM_001171812.2:c.1341T>C	NP_001165283.1:p.Val447=