Canonical Allele Identifier: CA1355976994
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997343C= , CM000665.2:g.32997343C= GRCh38
NC_000003.11:g.33038835C= , CM000665.1:g.33038835C= GRCh37
NC_000003.10:g.33013839C= NCBI36
NG_009005.1:g.104860G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1736G= MANE Select ENSP00000306920.4:p.Gly579=
ENST00000307363.9:c.1736G= ENSP00000306920.4:p.Gly579=
ENST00000307377.12:c.1343G= ENSP00000305920.8:p.Gly448=
ENST00000399402.7:c.1646G= ENSP00000382333.2:p.Gly549=
NM_000404.2:c.1736G= NP_000395.2:p.Gly579=
NM_000404.3:c.1736G= NP_000395.2:p.Gly579=
NM_001079811.1:c.1646G= NP_001073279.1:p.Gly549=
NM_001079811.2:c.1646G= NP_001073279.1:p.Gly549=
NM_001135602.1:c.1343G= NP_001129074.1:p.Gly448=
NM_001135602.2:c.1343G= NP_001129074.1:p.Gly448=
NM_001317040.1:c.1880G= NP_001303969.1:p.Gly627=
NM_000404.4:c.1736G= MANE Select NP_000395.3:p.Gly579=
NM_001079811.3:c.1646G= NP_001073279.2:p.Gly549=
NM_001135602.3:c.1343G= NP_001129074.2:p.Gly448=
NM_001317040.2:c.1880G= NP_001303969.2:p.Gly627=
NM_001393580.1:c.1734+16713G= NP_001380509.1:n.1734+16713G=