Canonical Allele Identifier: CA1355976982

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997308A= , CM000665.2:g.32997308A=	GRCh38
NC_000003.11:g.33038800A= , CM000665.1:g.33038800A=	GRCh37
NC_000003.10:g.33013804A=	NCBI36
NG_009005.1:g.104895T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.1771T= MANE Select	NP_000395.3:p.Tyr591=
ENST00000307363.10:c.1771T= MANE Select	ENSP00000306920.4:p.Tyr591=
NM_000404.2:c.1771T=	NP_000395.2:p.Tyr591=
NM_000404.3:c.1771T=	NP_000395.2:p.Tyr591=
NM_001079811.1:c.1681T=	NP_001073279.1:p.Tyr561=
NM_001079811.2:c.1681T=	NP_001073279.1:p.Tyr561=
NM_001079811.3:c.1681T=	NP_001073279.2:p.Tyr561=
NM_001135602.1:c.1378T=	NP_001129074.1:p.Tyr460=
NM_001135602.2:c.1378T=	NP_001129074.1:p.Tyr460=
NM_001135602.3:c.1378T=	NP_001129074.2:p.Tyr460=
NM_001317040.1:c.1915T=	NP_001303969.1:p.Tyr639=
NM_001317040.2:c.1915T=	NP_001303969.2:p.Tyr639=
NM_001393580.1:c.1734+16748T=	NP_001380509.1:n.1734+16748T=
ENST00000307363.9:c.1771T=	ENSP00000306920.4:p.Tyr591=
ENST00000307377.12:c.1378T=	ENSP00000305920.8:p.Tyr460=
ENST00000399402.7:c.1681T=	ENSP00000382333.2:p.Tyr561=