Canonical Allele Identifier: CA1355976983
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997310C= , CM000665.2:g.32997310C= GRCh38
NC_000003.11:g.33038802C= , CM000665.1:g.33038802C= GRCh37
NC_000003.10:g.33013806C= NCBI36
NG_009005.1:g.104893G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307363.10:c.1769G= MANE Select ENSP00000306920.4:p.Arg590=
ENST00000307363.9:c.1769G= ENSP00000306920.4:p.Arg590=
ENST00000307377.12:c.1376G= ENSP00000305920.8:p.Arg459=
ENST00000399402.7:c.1679G= ENSP00000382333.2:p.Arg560=
NM_000404.2:c.1769G= NP_000395.2:p.Arg590=
NM_000404.3:c.1769G= NP_000395.2:p.Arg590=
NM_001079811.1:c.1679G= NP_001073279.1:p.Arg560=
NM_001079811.2:c.1679G= NP_001073279.1:p.Arg560=
NM_001135602.1:c.1376G= NP_001129074.1:p.Arg459=
NM_001135602.2:c.1376G= NP_001129074.1:p.Arg459=
NM_001317040.1:c.1913G= NP_001303969.1:p.Arg638=
NM_000404.4:c.1769G= MANE Select NP_000395.3:p.Arg590=
NM_001079811.3:c.1679G= NP_001073279.2:p.Arg560=
NM_001135602.3:c.1376G= NP_001129074.2:p.Arg459=
NM_001317040.2:c.1913G= NP_001303969.2:p.Arg638=
NM_001393580.1:c.1734+16746G= NP_001380509.1:n.1734+16746G=