Canonical Allele Identifier: CA1355976944
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997212A= , CM000665.2:g.32997212A= GRCh38
NC_000003.11:g.33038704A= , CM000665.1:g.33038704A= GRCh37
NC_000003.10:g.33013708A= NCBI36
NG_009005.1:g.104991T=

Transcript Alleles

HGVS Amino-acid change
ENST00000307363.10:c.1867T= MANE Select ENSP00000306920.4:p.Trp623=
ENST00000307363.9:c.1867T= ENSP00000306920.4:p.Trp623=
ENST00000307377.12:c.1474T= ENSP00000305920.8:p.Trp492=
ENST00000399402.7:c.1777T= ENSP00000382333.2:p.Trp593=
NM_000404.2:c.1867T= NP_000395.2:p.Trp623=
NM_000404.3:c.1867T= NP_000395.2:p.Trp623=
NM_001079811.1:c.1777T= NP_001073279.1:p.Trp593=
NM_001079811.2:c.1777T= NP_001073279.1:p.Trp593=
NM_001135602.1:c.1474T= NP_001129074.1:p.Trp492=
NM_001135602.2:c.1474T= NP_001129074.1:p.Trp492=
NM_001317040.1:c.2011T= NP_001303969.1:p.Trp671=
NM_000404.4:c.1867T= MANE Select NP_000395.3:p.Trp623=
NM_001079811.3:c.1777T= NP_001073279.2:p.Trp593=
NM_001135602.3:c.1474T= NP_001129074.2:p.Trp492=
NM_001317040.2:c.2011T= NP_001303969.2:p.Trp671=
NM_001393580.1:c.1734+16844T= NP_001380509.1:n.1734+16844T=