Canonical Allele Identifier: CA2299354
Community Standard Title: NM_000404.4(GLB1):c.1580G>A (p.Trp527Ter)
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33014210C>T , CM000665.2:g.33014210C>T GRCh38
NC_000003.11:g.33055702C>T , CM000665.1:g.33055702C>T GRCh37
NC_000003.10:g.33030706C>T NCBI36
NG_009005.1:g.87993G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000404.4:c.1580G>A MANE Select NP_000395.3:p.Trp527Ter
ENST00000307363.10:c.1580G>A MANE Select ENSP00000306920.4:p.Trp527Ter
NM_000404.2:c.1580G>A NP_000395.2:p.Trp527Ter
NM_000404.3:c.1580G>A NP_000395.2:p.Trp527Ter
NM_001079811.1:c.1490G>A NP_001073279.1:p.Trp497Ter
NM_001079811.2:c.1490G>A NP_001073279.1:p.Trp497Ter
NM_001079811.3:c.1490G>A NP_001073279.2:p.Trp497Ter
NM_001135602.1:c.1187G>A NP_001129074.1:p.Trp396Ter
NM_001135602.2:c.1187G>A NP_001129074.1:p.Trp396Ter
NM_001135602.3:c.1187G>A NP_001129074.2:p.Trp396Ter
NM_001317040.1:c.1724G>A NP_001303969.1:p.Trp575Ter
NM_001317040.2:c.1724G>A NP_001303969.2:p.Trp575Ter
NM_001393580.1:c.1580G>A NP_001380509.1:p.Trp527Ter
ENST00000307363.9:c.1580G>A ENSP00000306920.4:p.Trp527Ter
ENST00000307377.12:c.1187G>A ENSP00000305920.8:p.Trp396Ter
ENST00000399402.7:c.1490G>A ENSP00000382333.2:p.Trp497Ter
ENST00000461475.5:n.679G>A
ENST00000497796.5:n.832G>A