Canonical Allele Identifier: CA342713973
Community Standard Title: NM_000157.4(GBA1):c.1249T>G (p.Trp417Gly)
Gene: GBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155235820A>C , CM000663.2:g.155235820A>C GRCh38
NC_000001.10:g.155205611A>C , CM000663.1:g.155205611A>C GRCh37
NC_000001.9:g.153472235A>C NCBI36
NG_009783.1:g.13878T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000157.4:c.1249T>G MANE Select NP_000148.2:p.Trp417Gly
ENST00000368373.8:c.1249T>G MANE Select ENSP00000357357.3:p.Trp417Gly
NM_000157.3:c.1249T>G NP_000148.2:p.Trp417Gly
NM_001005741.2:c.1249T>G NP_001005741.1:p.Trp417Gly
NM_001005741.3:c.1249T>G NP_001005741.1:p.Trp417Gly
NM_001005742.2:c.1249T>G NP_001005742.1:p.Trp417Gly
NM_001005742.3:c.1249T>G NP_001005742.1:p.Trp417Gly
NM_001171811.1:c.988T>G NP_001165282.1:p.Trp330Gly
NM_001171811.2:c.988T>G NP_001165282.1:p.Trp330Gly
NM_001171812.1:c.1102T>G NP_001165283.1:p.Trp368Gly
NM_001171812.2:c.1102T>G NP_001165283.1:p.Trp368Gly
ENST00000327247.9:c.1249T>G ENSP00000314508.5:p.Trp417Gly
ENST00000368373.7:c.1249T>G ENSP00000357357.3:p.Trp417Gly
ENST00000427500.7:c.1102T>G ENSP00000402577.2:p.Trp368Gly
ENST00000428024.3:c.988T>G ENSP00000397986.2:p.Trp330Gly
ENST00000464536.1:n.16T>G
ENST00000478472.1:n.240T>G
ENST00000484489.5:n.408T>G
XM_006711270.1:c.1249T>G XP_006711333.1:p.Trp417Gly
XM_011509407.1:c.1249T>G XP_011507709.1:p.Trp417Gly