Canonical Allele Identifier: CA1356008937

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33068651G= , CM000665.2:g.33068651G=	GRCh38
NC_000003.11:g.33110143G= , CM000665.1:g.33110143G=	GRCh37
NC_000003.10:g.33085147G=	NCBI36
NG_009005.1:g.33552C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.396+169C= MANE Select	ENSP00000306920.4:n.396+169C=
ENST00000307363.9:c.396+169C=	ENSP00000306920.4:n.396+169C=
ENST00000307377.12:c.246-3094C=	ENSP00000305920.8:n.246-3094C=
ENST00000399402.7:c.306+169C=	ENSP00000382333.2:n.306+169C=
ENST00000415454.1:c.76-10382C=	ENSP00000411813.1:n.76-10382C=
ENST00000438227.1:c.76-3094C=	ENSP00000401250.1:n.76-3094C=
ENST00000440656.1:c.3+169C=	ENSP00000411769.1:n.3+169C=
ENST00000446732.5:c.156-3094C=	ENSP00000407365.1:n.156-3094C=
ENST00000464355.1:n.354+169C=
ENST00000482097.5:n.109-15102C=
ENST00000485698.5:n.137-15102C=
ENST00000498537.5:n.133-15102C=
NM_000404.2:c.396+169C=	NP_000395.2:n.396+169C=
NM_000404.3:c.396+169C=	NP_000395.2:n.396+169C=
NM_001079811.1:c.306+169C=	NP_001073279.1:n.306+169C=
NM_001079811.2:c.306+169C=	NP_001073279.1:n.306+169C=
NM_001135602.1:c.246-3094C=	NP_001129074.1:n.246-3094C=
NM_001135602.2:c.246-3094C=	NP_001129074.1:n.246-3094C=
NM_001317040.1:c.540+169C=	NP_001303969.1:n.540+169C=
NM_000404.4:c.396+169C= MANE Select	NP_000395.3:n.396+169C=
NM_001079811.3:c.306+169C=	NP_001073279.2:n.306+169C=
NM_001135602.3:c.246-3094C=	NP_001129074.2:n.246-3094C=
NM_001317040.2:c.540+169C=	NP_001303969.2:n.540+169C=
NM_001393580.1:c.396+169C=	NP_001380509.1:n.396+169C=