Canonical Allele Identifier: CA1355998416

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33046137G= , CM000665.2:g.33046137G=	GRCh38
NC_000003.11:g.33087629G= , CM000665.1:g.33087629G=	GRCh37
NC_000003.10:g.33062633G=	NCBI36
NG_009005.1:g.56066C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.1051C= MANE Select	NP_000395.3:p.Arg351=
ENST00000307363.10:c.1051C= MANE Select	ENSP00000306920.4:p.Arg351=
NM_000404.2:c.1051C=	NP_000395.2:p.Arg351=
NM_000404.3:c.1051C=	NP_000395.2:p.Arg351=
NM_001079811.1:c.961C=	NP_001073279.1:p.Arg321=
NM_001079811.2:c.961C=	NP_001073279.1:p.Arg321=
NM_001079811.3:c.961C=	NP_001073279.2:p.Arg321=
NM_001135602.1:c.658C=	NP_001129074.1:p.Arg220=
NM_001135602.2:c.658C=	NP_001129074.1:p.Arg220=
NM_001135602.3:c.658C=	NP_001129074.2:p.Arg220=
NM_001317040.1:c.1195C=	NP_001303969.1:p.Arg399=
NM_001317040.2:c.1195C=	NP_001303969.2:p.Arg399=
NM_001393580.1:c.1051C=	NP_001380509.1:p.Arg351=
ENST00000307363.9:c.1051C=	ENSP00000306920.4:p.Arg351=
ENST00000307377.12:c.658C=	ENSP00000305920.8:p.Arg220=
ENST00000399402.7:c.961C=	ENSP00000382333.2:p.Arg321=
ENST00000482097.5:n.426C=
ENST00000485698.5:n.454C=
ENST00000490658.2:n.56C=