Canonical Allele Identifier: CA1355986175
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33018493T= , CM000665.2:g.33018493T= GRCh38
NC_000003.11:g.33059985T= , CM000665.1:g.33059985T= GRCh37
NC_000003.10:g.33034989T= NCBI36
NG_009005.1:g.83710A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1302A= MANE Select ENSP00000306920.4:p.Ser434=
ENST00000307363.9:c.1302A= ENSP00000306920.4:p.Ser434=
ENST00000307377.12:c.909A= ENSP00000305920.8:p.Ser303=
ENST00000399402.7:c.1212A= ENSP00000382333.2:p.Ser404=
ENST00000461475.5:n.401A=
ENST00000467571.5:n.339A=
ENST00000497796.5:n.554A=
NM_000404.2:c.1302A= NP_000395.2:p.Ser434=
NM_000404.3:c.1302A= NP_000395.2:p.Ser434=
NM_001079811.1:c.1212A= NP_001073279.1:p.Ser404=
NM_001079811.2:c.1212A= NP_001073279.1:p.Ser404=
NM_001135602.1:c.909A= NP_001129074.1:p.Ser303=
NM_001135602.2:c.909A= NP_001129074.1:p.Ser303=
NM_001317040.1:c.1446A= NP_001303969.1:p.Ser482=
NM_000404.4:c.1302A= MANE Select NP_000395.3:p.Ser434=
NM_001079811.3:c.1212A= NP_001073279.2:p.Ser404=
NM_001135602.3:c.909A= NP_001129074.2:p.Ser303=
NM_001317040.2:c.1446A= NP_001303969.2:p.Ser482=
NM_001393580.1:c.1302A= NP_001380509.1:p.Ser434=