Canonical Allele Identifier: CA1355976979

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997296G= , CM000665.2:g.32997296G=	GRCh38
NC_000003.11:g.33038788G= , CM000665.1:g.33038788G=	GRCh37
NC_000003.10:g.33013792G=	NCBI36
NG_009005.1:g.104907C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1783C= MANE Select	ENSP00000306920.4:p.Arg595=
ENST00000307363.9:c.1783C=	ENSP00000306920.4:p.Arg595=
ENST00000307377.12:c.1390C=	ENSP00000305920.8:p.Arg464=
ENST00000399402.7:c.1693C=	ENSP00000382333.2:p.Arg565=
NM_000404.2:c.1783C=	NP_000395.2:p.Arg595=
NM_000404.3:c.1783C=	NP_000395.2:p.Arg595=
NM_001079811.1:c.1693C=	NP_001073279.1:p.Arg565=
NM_001079811.2:c.1693C=	NP_001073279.1:p.Arg565=
NM_001135602.1:c.1390C=	NP_001129074.1:p.Arg464=
NM_001135602.2:c.1390C=	NP_001129074.1:p.Arg464=
NM_001317040.1:c.1927C=	NP_001303969.1:p.Arg643=
NM_000404.4:c.1783C= MANE Select	NP_000395.3:p.Arg595=
NM_001079811.3:c.1693C=	NP_001073279.2:p.Arg565=
NM_001135602.3:c.1390C=	NP_001129074.2:p.Arg464=
NM_001317040.2:c.1927C=	NP_001303969.2:p.Arg643=
NM_001393580.1:c.1734+16760C=	NP_001380509.1:n.1734+16760C=