Canonical Allele Identifier: CA1356008768

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33068245G= , CM000665.2:g.33068245G=	GRCh38
NC_000003.11:g.33109737G= , CM000665.1:g.33109737G=	GRCh37
NC_000003.10:g.33084741G=	NCBI36
NG_009005.1:g.33958C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.442C= MANE Select	NP_000395.3:p.Arg148=
ENST00000307363.10:c.442C= MANE Select	ENSP00000306920.4:p.Arg148=
NM_000404.2:c.442C=	NP_000395.2:p.Arg148=
NM_000404.3:c.442C=	NP_000395.2:p.Arg148=
NM_001079811.1:c.352C=	NP_001073279.1:p.Arg118=
NM_001079811.2:c.352C=	NP_001073279.1:p.Arg118=
NM_001079811.3:c.352C=	NP_001073279.2:p.Arg118=
NM_001135602.1:c.246-2688C=	NP_001129074.1:n.246-2688C=
NM_001135602.2:c.246-2688C=	NP_001129074.1:n.246-2688C=
NM_001135602.3:c.246-2688C=	NP_001129074.2:n.246-2688C=
NM_001317040.1:c.586C=	NP_001303969.1:p.Arg196=
NM_001317040.2:c.586C=	NP_001303969.2:p.Arg196=
NM_001393580.1:c.442C=	NP_001380509.1:p.Arg148=
ENST00000307363.9:c.442C=	ENSP00000306920.4:p.Arg148=
ENST00000307377.12:c.246-2688C=	ENSP00000305920.8:n.246-2688C=
ENST00000399402.7:c.352C=	ENSP00000382333.2:p.Arg118=
ENST00000415454.1:c.76-9976C=	ENSP00000411813.1:n.76-9976C=
ENST00000438227.1:c.76-2688C=	ENSP00000401250.1:n.76-2688C=
ENST00000440656.1:c.49C=	ENSP00000411769.1:p.Arg17=
ENST00000446732.5:c.156-2688C=	ENSP00000407365.1:n.156-2688C=
ENST00000464355.1:n.400C=
ENST00000482097.5:n.109-14696C=
ENST00000485698.5:n.137-14696C=
ENST00000498537.5:n.133-14696C=