Canonical Allele Identifier: CA1355976911

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997127T= , CM000665.2:g.32997127T=	GRCh38
NC_000003.11:g.33038619T= , CM000665.1:g.33038619T=	GRCh37
NC_000003.10:g.33013623T=	NCBI36
NG_009005.1:g.105076A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1952A= MANE Select	ENSP00000306920.4:p.Asp651=
ENST00000307363.9:c.1952A=	ENSP00000306920.4:p.Asp651=
ENST00000307377.12:c.1559A=	ENSP00000305920.8:p.Asp520=
ENST00000399402.7:c.1862A=	ENSP00000382333.2:p.Asp621=
NM_000404.2:c.1952A=	NP_000395.2:p.Asp651=
NM_000404.3:c.1952A=	NP_000395.2:p.Asp651=
NM_001079811.1:c.1862A=	NP_001073279.1:p.Asp621=
NM_001079811.2:c.1862A=	NP_001073279.1:p.Asp621=
NM_001135602.1:c.1559A=	NP_001129074.1:p.Asp520=
NM_001135602.2:c.1559A=	NP_001129074.1:p.Asp520=
NM_001317040.1:c.2096A=	NP_001303969.1:p.Asp699=
NM_000404.4:c.1952A= MANE Select	NP_000395.3:p.Asp651=
NM_001079811.3:c.1862A=	NP_001073279.2:p.Asp621=
NM_001135602.3:c.1559A=	NP_001129074.2:p.Asp520=
NM_001317040.2:c.2096A=	NP_001303969.2:p.Asp699=
NM_001393580.1:c.1734+16929A=	NP_001380509.1:n.1734+16929A=