Canonical Allele Identifier: CA342719584
Community Standard Title: NM_000157.4(GBA1):c.886C>T (p.Arg296Ter)
Gene: GBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155237454G>A , CM000663.2:g.155237454G>A GRCh38
NC_000001.10:g.155207245G>A , CM000663.1:g.155207245G>A GRCh37
NC_000001.9:g.153473869G>A NCBI36
NG_009783.1:g.12244C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000157.4:c.886C>T MANE Select NP_000148.2:p.Arg296Ter
ENST00000368373.8:c.886C>T MANE Select ENSP00000357357.3:p.Arg296Ter
NM_000157.3:c.886C>T NP_000148.2:p.Arg296Ter
NM_001005741.2:c.886C>T NP_001005741.1:p.Arg296Ter
NM_001005741.3:c.886C>T NP_001005741.1:p.Arg296Ter
NM_001005742.2:c.886C>T NP_001005742.1:p.Arg296Ter
NM_001005742.3:c.886C>T NP_001005742.1:p.Arg296Ter
NM_001171811.1:c.625C>T NP_001165282.1:p.Arg209Ter
NM_001171811.2:c.625C>T NP_001165282.1:p.Arg209Ter
NM_001171812.1:c.739C>T NP_001165283.1:p.Arg247Ter
NM_001171812.2:c.739C>T NP_001165283.1:p.Arg247Ter
ENST00000327247.9:c.886C>T ENSP00000314508.5:p.Arg296Ter
ENST00000368373.7:c.886C>T ENSP00000357357.3:p.Arg296Ter
ENST00000427500.7:c.739C>T ENSP00000402577.2:p.Arg247Ter
ENST00000428024.3:c.625C>T ENSP00000397986.2:p.Arg209Ter
ENST00000484489.5:n.340-1166C>T
ENST00000491081.5:n.491C>T
ENST00000497670.5:n.509C>T
XM_006711270.1:c.886C>T XP_006711333.1:p.Arg296Ter
XM_011509407.1:c.886C>T XP_011507709.1:p.Arg296Ter