Canonical Allele Identifier: CA2586971831
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997240dup , CM000665.2:g.32997240dup GRCh38
NC_000003.11:g.33038732dup , CM000665.1:g.33038732dup GRCh37
NC_000003.10:g.33013736dup NCBI36
NG_009005.1:g.104965dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1841dup MANE Select ENSP00000306920.4:p.Asn614LysfsTer16
ENST00000307363.9:c.1841dup ENSP00000306920.4:p.Asn614LysfsTer16
ENST00000307377.12:c.1448dup ENSP00000305920.8:p.Asn483LysfsTer16
ENST00000399402.7:c.1751dup ENSP00000382333.2:p.Asn584LysfsTer16
NM_000404.2:c.1841dup NP_000395.2:p.Asn614LysfsTer16
NM_000404.3:c.1841dup NP_000395.2:p.Asn614LysfsTer16
NM_001079811.1:c.1751dup NP_001073279.1:p.Asn584LysfsTer16
NM_001079811.2:c.1751dup NP_001073279.1:p.Asn584LysfsTer16
NM_001135602.1:c.1448dup NP_001129074.1:p.Asn483LysfsTer16
NM_001135602.2:c.1448dup NP_001129074.1:p.Asn483LysfsTer16
NM_001317040.1:c.1985dup NP_001303969.1:p.Asn662LysfsTer16
NM_000404.4:c.1841dup MANE Select NP_000395.3:p.Asn614LysfsTer16
NM_001079811.3:c.1751dup NP_001073279.2:p.Asn584LysfsTer16
NM_001135602.3:c.1448dup NP_001129074.2:p.Asn483LysfsTer16
NM_001317040.2:c.1985dup NP_001303969.2:p.Asn662LysfsTer16
NM_001393580.1:c.1734+16818dup NP_001380509.1:n.1734+16818dup