Canonical Allele Identifier: CA1355976986
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997313C= , CM000665.2:g.32997313C= GRCh38
NC_000003.11:g.33038805C= , CM000665.1:g.33038805C= GRCh37
NC_000003.10:g.33013809C= NCBI36
NG_009005.1:g.104890G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307363.10:c.1766G= MANE Select ENSP00000306920.4:p.Gly589=
ENST00000307363.9:c.1766G= ENSP00000306920.4:p.Gly589=
ENST00000307377.12:c.1373G= ENSP00000305920.8:p.Gly458=
ENST00000399402.7:c.1676G= ENSP00000382333.2:p.Gly559=
NM_000404.2:c.1766G= NP_000395.2:p.Gly589=
NM_000404.3:c.1766G= NP_000395.2:p.Gly589=
NM_001079811.1:c.1676G= NP_001073279.1:p.Gly559=
NM_001079811.2:c.1676G= NP_001073279.1:p.Gly559=
NM_001135602.1:c.1373G= NP_001129074.1:p.Gly458=
NM_001135602.2:c.1373G= NP_001129074.1:p.Gly458=
NM_001317040.1:c.1910G= NP_001303969.1:p.Gly637=
NM_000404.4:c.1766G= MANE Select NP_000395.3:p.Gly589=
NM_001079811.3:c.1676G= NP_001073279.2:p.Gly559=
NM_001135602.3:c.1373G= NP_001129074.2:p.Gly458=
NM_001317040.2:c.1910G= NP_001303969.2:p.Gly637=
NM_001393580.1:c.1734+16743G= NP_001380509.1:n.1734+16743G=