Canonical Allele Identifier: CA1355987518

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33021600C= , CM000665.2:g.33021600C=	GRCh38
NC_000003.11:g.33063092C= , CM000665.1:g.33063092C=	GRCh37
NC_000003.10:g.33038096C=	NCBI36
NG_009005.1:g.80603G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1199G= MANE Select	ENSP00000306920.4:p.Ser400=
ENST00000307363.9:c.1199G=	ENSP00000306920.4:p.Ser400=
ENST00000307377.12:c.806G=	ENSP00000305920.8:p.Ser269=
ENST00000399402.7:c.1109G=	ENSP00000382333.2:p.Ser370=
ENST00000461475.5:n.298G=
ENST00000467571.5:n.236G=
ENST00000473477.1:n.231G=
ENST00000497796.5:n.451G=
NM_000404.2:c.1199G=	NP_000395.2:p.Ser400=
NM_000404.3:c.1199G=	NP_000395.2:p.Ser400=
NM_001079811.1:c.1109G=	NP_001073279.1:p.Ser370=
NM_001079811.2:c.1109G=	NP_001073279.1:p.Ser370=
NM_001135602.1:c.806G=	NP_001129074.1:p.Ser269=
NM_001135602.2:c.806G=	NP_001129074.1:p.Ser269=
NM_001317040.1:c.1343G=	NP_001303969.1:p.Ser448=
XR_001740634.1:n.1543-588C=
NM_000404.4:c.1199G= MANE Select	NP_000395.3:p.Ser400=
NM_001079811.3:c.1109G=	NP_001073279.2:p.Ser370=
NM_001135602.3:c.806G=	NP_001129074.2:p.Ser269=
NM_001317040.2:c.1343G=	NP_001303969.2:p.Ser448=
NM_001393580.1:c.1199G=	NP_001380509.1:p.Ser400=