Canonical Allele Identifier: CA1356009002

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33068789A= , CM000665.2:g.33068789A=	GRCh38
NC_000003.11:g.33110281A= , CM000665.1:g.33110281A=	GRCh37
NC_000003.10:g.33085285A=	NCBI36
NG_009005.1:g.33414T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.396+31T= MANE Select	ENSP00000306920.4:n.396+31T=
ENST00000307363.9:c.396+31T=	ENSP00000306920.4:n.396+31T=
ENST00000307377.12:c.246-3232T=	ENSP00000305920.8:n.246-3232T=
ENST00000399402.7:c.306+31T=	ENSP00000382333.2:n.306+31T=
ENST00000415454.1:c.76-10520T=	ENSP00000411813.1:n.76-10520T=
ENST00000438227.1:c.76-3232T=	ENSP00000401250.1:n.76-3232T=
ENST00000440656.1:c.3+31T=	ENSP00000411769.1:n.3+31T=
ENST00000446732.5:c.156-3232T=	ENSP00000407365.1:n.156-3232T=
ENST00000464355.1:n.354+31T=
ENST00000482097.5:n.109-15240T=
ENST00000485698.5:n.137-15240T=
ENST00000498537.5:n.133-15240T=
NM_000404.2:c.396+31T=	NP_000395.2:n.396+31T=
NM_000404.3:c.396+31T=	NP_000395.2:n.396+31T=
NM_001079811.1:c.306+31T=	NP_001073279.1:n.306+31T=
NM_001079811.2:c.306+31T=	NP_001073279.1:n.306+31T=
NM_001135602.1:c.246-3232T=	NP_001129074.1:n.246-3232T=
NM_001135602.2:c.246-3232T=	NP_001129074.1:n.246-3232T=
NM_001317040.1:c.540+31T=	NP_001303969.1:n.540+31T=
NM_000404.4:c.396+31T= MANE Select	NP_000395.3:n.396+31T=
NM_001079811.3:c.306+31T=	NP_001073279.2:n.306+31T=
NM_001135602.3:c.246-3232T=	NP_001129074.2:n.246-3232T=
NM_001317040.2:c.540+31T=	NP_001303969.2:n.540+31T=
NM_001393580.1:c.396+31T=	NP_001380509.1:n.396+31T=