Canonical Allele Identifier: CA421025570

Gene: GBA1

Linked Data

• MyVariant Identifiers: chr1:g.155207951G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238160G>A , CM000663.2:g.155238160G>A	GRCh38
NC_000001.10:g.155207951G>A , CM000663.1:g.155207951G>A	GRCh37
NC_000001.9:g.153474575G>A	NCBI36
NG_009783.1:g.11538C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368373.8:c.735C>T MANE Select	ENSP00000357357.3:p.His245=
ENST00000327247.9:c.735C>T	ENSP00000314508.5:p.His245=
ENST00000368373.7:c.735C>T	ENSP00000357357.3:p.His245=
ENST00000427500.7:c.588C>T	ENSP00000402577.2:p.His196=
ENST00000428024.3:c.474C>T	ENSP00000397986.2:p.His158=
ENST00000460156.1:n.522C>T
ENST00000484489.5:n.339+1813C>T
ENST00000491081.5:n.340C>T
ENST00000497670.5:n.358C>T
NM_000157.3:c.735C>T	NP_000148.2:p.His245=
NM_001005741.2:c.735C>T	NP_001005741.1:p.His245=
NM_001005742.2:c.735C>T	NP_001005742.1:p.His245=
NM_001171811.1:c.474C>T	NP_001165282.1:p.His158=
NM_001171812.1:c.588C>T	NP_001165283.1:p.His196=
XM_006711270.1:c.735C>T	XP_006711333.1:p.His245=
XM_011509407.1:c.735C>T	XP_011507709.1:p.His245=
NM_000157.4:c.735C>T MANE Select	NP_000148.2:p.His245=
NM_001005741.3:c.735C>T	NP_001005741.1:p.His245=
NM_001005742.3:c.735C>T	NP_001005742.1:p.His245=
NM_001171811.2:c.474C>T	NP_001165282.1:p.His158=
NM_001171812.2:c.588C>T	NP_001165283.1:p.His196=