Canonical Allele Identifier: CA1355976978

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997295C= , CM000665.2:g.32997295C=	GRCh38
NC_000003.11:g.33038787C= , CM000665.1:g.33038787C=	GRCh37
NC_000003.10:g.33013791C=	NCBI36
NG_009005.1:g.104908G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1784G= MANE Select	ENSP00000306920.4:p.Arg595=
ENST00000307363.9:c.1784G=	ENSP00000306920.4:p.Arg595=
ENST00000307377.12:c.1391G=	ENSP00000305920.8:p.Arg464=
ENST00000399402.7:c.1694G=	ENSP00000382333.2:p.Arg565=
NM_000404.2:c.1784G=	NP_000395.2:p.Arg595=
NM_000404.3:c.1784G=	NP_000395.2:p.Arg595=
NM_001079811.1:c.1694G=	NP_001073279.1:p.Arg565=
NM_001079811.2:c.1694G=	NP_001073279.1:p.Arg565=
NM_001135602.1:c.1391G=	NP_001129074.1:p.Arg464=
NM_001135602.2:c.1391G=	NP_001129074.1:p.Arg464=
NM_001317040.1:c.1928G=	NP_001303969.1:p.Arg643=
NM_000404.4:c.1784G= MANE Select	NP_000395.3:p.Arg595=
NM_001079811.3:c.1694G=	NP_001073279.2:p.Arg565=
NM_001135602.3:c.1391G=	NP_001129074.2:p.Arg464=
NM_001317040.2:c.1928G=	NP_001303969.2:p.Arg643=
NM_001393580.1:c.1734+16761G=	NP_001380509.1:n.1734+16761G=