Canonical Allele Identifier: CA1355984263

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33014057T= , CM000665.2:g.33014057T=	GRCh38
NC_000003.11:g.33055549T= , CM000665.1:g.33055549T=	GRCh37
NC_000003.10:g.33030553T=	NCBI36
NG_009005.1:g.88146A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.1733A= MANE Select	NP_000395.3:p.Lys578=
ENST00000307363.10:c.1733A= MANE Select	ENSP00000306920.4:p.Lys578=
NM_000404.2:c.1733A=	NP_000395.2:p.Lys578=
NM_000404.3:c.1733A=	NP_000395.2:p.Lys578=
NM_001079811.1:c.1643A=	NP_001073279.1:p.Lys548=
NM_001079811.2:c.1643A=	NP_001073279.1:p.Lys548=
NM_001079811.3:c.1643A=	NP_001073279.2:p.Lys548=
NM_001135602.1:c.1340A=	NP_001129074.1:p.Lys447=
NM_001135602.2:c.1340A=	NP_001129074.1:p.Lys447=
NM_001135602.3:c.1340A=	NP_001129074.2:p.Lys447=
NM_001317040.1:c.1877A=	NP_001303969.1:p.Lys626=
NM_001317040.2:c.1877A=	NP_001303969.2:p.Lys626=
NM_001393580.1:c.1733A=	NP_001380509.1:p.Lys578=
ENST00000307363.9:c.1733A=	ENSP00000306920.4:p.Lys578=
ENST00000307377.12:c.1340A=	ENSP00000305920.8:p.Lys447=
ENST00000399402.7:c.1643A=	ENSP00000382333.2:p.Lys548=