Canonical Allele Identifier: CA916865678
Gene: GLB1 HGNC NCBI

Linked Data

dbSNP Id: rs1559382010

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33014029del , CM000665.2:g.33014029del GRCh38
NC_000003.11:g.33055521del , CM000665.1:g.33055521del GRCh37
NC_000003.10:g.33030525del NCBI36
NG_009005.1:g.88175del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1734+28del MANE Select ENSP00000306920.4:n.1734+28del
ENST00000307363.9:c.1734+28del ENSP00000306920.4:n.1734+28del
ENST00000307377.12:c.1341+28del ENSP00000305920.8:n.1341+28del
ENST00000399402.7:c.1644+28del ENSP00000382333.2:n.1644+28del
NM_000404.2:c.1734+28del NP_000395.2:n.1734+28del
NM_000404.3:c.1734+28del NP_000395.2:n.1734+28del
NM_001079811.1:c.1644+28del NP_001073279.1:n.1644+28del
NM_001079811.2:c.1644+28del NP_001073279.1:n.1644+28del
NM_001135602.1:c.1341+28del NP_001129074.1:n.1341+28del
NM_001135602.2:c.1341+28del NP_001129074.1:n.1341+28del
NM_001317040.1:c.1878+28del NP_001303969.1:n.1878+28del
NM_000404.4:c.1734+28del MANE Select NP_000395.3:n.1734+28del
NM_001079811.3:c.1644+28del NP_001073279.2:n.1644+28del
NM_001135602.3:c.1341+28del NP_001129074.2:n.1341+28del
NM_001317040.2:c.1878+28del NP_001303969.2:n.1878+28del
NM_001393580.1:c.1734+28del NP_001380509.1:n.1734+28del