Canonical Allele Identifier: CA1355986178

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33018495A= , CM000665.2:g.33018495A=	GRCh38
NC_000003.11:g.33059987A= , CM000665.1:g.33059987A=	GRCh37
NC_000003.10:g.33034991A=	NCBI36
NG_009005.1:g.83708T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1300T= MANE Select	ENSP00000306920.4:p.Ser434=
ENST00000307363.9:c.1300T=	ENSP00000306920.4:p.Ser434=
ENST00000307377.12:c.907T=	ENSP00000305920.8:p.Ser303=
ENST00000399402.7:c.1210T=	ENSP00000382333.2:p.Ser404=
ENST00000461475.5:n.399T=
ENST00000467571.5:n.337T=
ENST00000497796.5:n.552T=
NM_000404.2:c.1300T=	NP_000395.2:p.Ser434=
NM_000404.3:c.1300T=	NP_000395.2:p.Ser434=
NM_001079811.1:c.1210T=	NP_001073279.1:p.Ser404=
NM_001079811.2:c.1210T=	NP_001073279.1:p.Ser404=
NM_001135602.1:c.907T=	NP_001129074.1:p.Ser303=
NM_001135602.2:c.907T=	NP_001129074.1:p.Ser303=
NM_001317040.1:c.1444T=	NP_001303969.1:p.Ser482=
NM_000404.4:c.1300T= MANE Select	NP_000395.3:p.Ser434=
NM_001079811.3:c.1210T=	NP_001073279.2:p.Ser404=
NM_001135602.3:c.907T=	NP_001129074.2:p.Ser303=
NM_001317040.2:c.1444T=	NP_001303969.2:p.Ser482=
NM_001393580.1:c.1300T=	NP_001380509.1:p.Ser434=