Canonical Allele Identifier: CA351999799
Gene: GLB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997045T>A , CM000665.2:g.32997045T>A GRCh38
NC_000003.11:g.33038537T>A , CM000665.1:g.33038537T>A GRCh37
NC_000003.10:g.33013541T>A NCBI36
NG_009005.1:g.105158A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.2034A>T MANE Select ENSP00000306920.4:p.Ter678Cys
ENST00000307363.9:c.2034A>T ENSP00000306920.4:p.Ter678Cys
ENST00000307377.12:c.1641A>T ENSP00000305920.8:p.Ter547Cys
ENST00000399402.7:c.1944A>T ENSP00000382333.2:p.Ter648Cys
NM_000404.2:c.2034A>T NP_000395.2:p.Ter678Cys
NM_000404.3:c.2034A>T NP_000395.2:p.Ter678Cys
NM_001079811.1:c.1944A>T NP_001073279.1:p.Ter648Cys
NM_001079811.2:c.1944A>T NP_001073279.1:p.Ter648Cys
NM_001135602.1:c.1641A>T NP_001129074.1:p.Ter547Cys
NM_001135602.2:c.1641A>T NP_001129074.1:p.Ter547Cys
NM_001317040.1:c.2178A>T NP_001303969.1:p.Ter726Cys
NM_000404.4:c.2034A>T MANE Select NP_000395.3:p.Ter678Cys
NM_001079811.3:c.1944A>T NP_001073279.2:p.Ter648Cys
NM_001135602.3:c.1641A>T NP_001129074.2:p.Ter547Cys
NM_001317040.2:c.2178A>T NP_001303969.2:p.Ter726Cys
NM_001393580.1:c.1734+17011A>T NP_001380509.1:n.1734+17011A>T