Canonical Allele Identifier: CA1355986118
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33018390A= , CM000665.2:g.33018390A= GRCh38
NC_000003.11:g.33059882A= , CM000665.1:g.33059882A= GRCh37
NC_000003.10:g.33034886A= NCBI36
NG_009005.1:g.83813T=

Transcript Alleles

HGVS Amino-acid change
ENST00000307363.10:c.1347+58T= MANE Select ENSP00000306920.4:n.1347+58T=
ENST00000307363.9:c.1347+58T= ENSP00000306920.4:n.1347+58T=
ENST00000307377.12:c.954+58T= ENSP00000305920.8:n.954+58T=
ENST00000399402.7:c.1257+58T= ENSP00000382333.2:n.1257+58T=
ENST00000461475.5:n.446+58T=
ENST00000467571.5:n.384+58T=
ENST00000497796.5:n.599+58T=
NM_000404.2:c.1347+58T= NP_000395.2:n.1347+58T=
NM_000404.3:c.1347+58T= NP_000395.2:n.1347+58T=
NM_001079811.1:c.1257+58T= NP_001073279.1:n.1257+58T=
NM_001079811.2:c.1257+58T= NP_001073279.1:n.1257+58T=
NM_001135602.1:c.954+58T= NP_001129074.1:n.954+58T=
NM_001135602.2:c.954+58T= NP_001129074.1:n.954+58T=
NM_001317040.1:c.1491+58T= NP_001303969.1:n.1491+58T=
NM_000404.4:c.1347+58T= MANE Select NP_000395.3:n.1347+58T=
NM_001079811.3:c.1257+58T= NP_001073279.2:n.1257+58T=
NM_001135602.3:c.954+58T= NP_001129074.2:n.954+58T=
NM_001317040.2:c.1491+58T= NP_001303969.2:n.1491+58T=
NM_001393580.1:c.1347+58T= NP_001380509.1:n.1347+58T=