Canonical Allele Identifier: CA10586860
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33014229A= , CM000665.2:g.33014229A= GRCh38
NC_000003.11:g.33055721A= , CM000665.1:g.33055721A= GRCh37
NC_000003.10:g.33030725A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1561T= MANE Select ENSP00000306920.4:p.Cys521=
ENST00000307363.9:c.1561T= ENSP00000306920.4:p.Cys521=
ENST00000307377.12:c.1168T= ENSP00000305920.8:p.Cys390=
ENST00000399402.7:c.1471T= ENSP00000382333.2:p.Cys491=
ENST00000461475.5:n.660T=
ENST00000497796.5:n.813T=
NM_000404.4:c.1561T= MANE Select NP_000395.3:p.Cys521=
NM_001079811.3:c.1471T= NP_001073279.2:p.Cys491=
NM_001135602.3:c.1168T= NP_001129074.2:p.Cys390=
NM_001317040.2:c.1705T= NP_001303969.2:p.Cys569=
NM_001393580.1:c.1561T= NP_001380509.1:p.Cys521=