Canonical Allele Identifier: CA1355976964
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997258G= , CM000665.2:g.32997258G= GRCh38
NC_000003.11:g.33038750G= , CM000665.1:g.33038750G= GRCh37
NC_000003.10:g.33013754G= NCBI36
NG_009005.1:g.104945C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1821C= MANE Select ENSP00000306920.4:p.Ile607=
ENST00000307363.9:c.1821C= ENSP00000306920.4:p.Ile607=
ENST00000307377.12:c.1428C= ENSP00000305920.8:p.Ile476=
ENST00000399402.7:c.1731C= ENSP00000382333.2:p.Ile577=
NM_000404.2:c.1821C= NP_000395.2:p.Ile607=
NM_000404.3:c.1821C= NP_000395.2:p.Ile607=
NM_001079811.1:c.1731C= NP_001073279.1:p.Ile577=
NM_001079811.2:c.1731C= NP_001073279.1:p.Ile577=
NM_001135602.1:c.1428C= NP_001129074.1:p.Ile476=
NM_001135602.2:c.1428C= NP_001129074.1:p.Ile476=
NM_001317040.1:c.1965C= NP_001303969.1:p.Ile655=
NM_000404.4:c.1821C= MANE Select NP_000395.3:p.Ile607=
NM_001079811.3:c.1731C= NP_001073279.2:p.Ile577=
NM_001135602.3:c.1428C= NP_001129074.2:p.Ile476=
NM_001317040.2:c.1965C= NP_001303969.2:p.Ile655=
NM_001393580.1:c.1734+16798C= NP_001380509.1:n.1734+16798C=