Canonical Allele Identifier: CA1355976946
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997218G= , CM000665.2:g.32997218G= GRCh38
NC_000003.11:g.33038710G= , CM000665.1:g.33038710G= GRCh37
NC_000003.10:g.33013714G= NCBI36
NG_009005.1:g.104985C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307363.10:c.1861C= MANE Select ENSP00000306920.4:p.Leu621=
ENST00000307363.9:c.1861C= ENSP00000306920.4:p.Leu621=
ENST00000307377.12:c.1468C= ENSP00000305920.8:p.Leu490=
ENST00000399402.7:c.1771C= ENSP00000382333.2:p.Leu591=
NM_000404.2:c.1861C= NP_000395.2:p.Leu621=
NM_000404.3:c.1861C= NP_000395.2:p.Leu621=
NM_001079811.1:c.1771C= NP_001073279.1:p.Leu591=
NM_001079811.2:c.1771C= NP_001073279.1:p.Leu591=
NM_001135602.1:c.1468C= NP_001129074.1:p.Leu490=
NM_001135602.2:c.1468C= NP_001129074.1:p.Leu490=
NM_001317040.1:c.2005C= NP_001303969.1:p.Leu669=
NM_000404.4:c.1861C= MANE Select NP_000395.3:p.Leu621=
NM_001079811.3:c.1771C= NP_001073279.2:p.Leu591=
NM_001135602.3:c.1468C= NP_001129074.2:p.Leu490=
NM_001317040.2:c.2005C= NP_001303969.2:p.Leu669=
NM_001393580.1:c.1734+16838C= NP_001380509.1:n.1734+16838C=