Canonical Allele Identifier: CA2664926657
Gene: GLB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997155del , CM000665.2:g.32997155del GRCh38
NC_000003.11:g.33038647del , CM000665.1:g.33038647del GRCh37
NC_000003.10:g.33013651del NCBI36
NG_009005.1:g.105049del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1925del MANE Select ENSP00000306920.4:p.Pro642GlnfsTer7
ENST00000307363.9:c.1925del ENSP00000306920.4:p.Pro642GlnfsTer7
ENST00000307377.12:c.1532del ENSP00000305920.8:p.Pro511GlnfsTer7
ENST00000399402.7:c.1835del ENSP00000382333.2:p.Pro612GlnfsTer7
NM_000404.2:c.1925del NP_000395.2:p.Pro642GlnfsTer7
NM_000404.3:c.1925del NP_000395.2:p.Pro642GlnfsTer7
NM_001079811.1:c.1835del NP_001073279.1:p.Pro612GlnfsTer7
NM_001079811.2:c.1835del NP_001073279.1:p.Pro612GlnfsTer7
NM_001135602.1:c.1532del NP_001129074.1:p.Pro511GlnfsTer7
NM_001135602.2:c.1532del NP_001129074.1:p.Pro511GlnfsTer7
NM_001317040.1:c.2069del NP_001303969.1:p.Pro690GlnfsTer7
NM_000404.4:c.1925del MANE Select NP_000395.3:p.Pro642GlnfsTer7
NM_001079811.3:c.1835del NP_001073279.2:p.Pro612GlnfsTer7
NM_001135602.3:c.1532del NP_001129074.2:p.Pro511GlnfsTer7
NM_001317040.2:c.2069del NP_001303969.2:p.Pro690GlnfsTer7
NM_001393580.1:c.1734+16902del NP_001380509.1:n.1734+16902del