Canonical Allele Identifier: CA1355987525

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33021612C= , CM000665.2:g.33021612C=	GRCh38
NC_000003.11:g.33063104C= , CM000665.1:g.33063104C=	GRCh37
NC_000003.10:g.33038108C=	NCBI36
NG_009005.1:g.80591G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1187G= MANE Select	ENSP00000306920.4:p.Gly396=
ENST00000307363.9:c.1187G=	ENSP00000306920.4:p.Gly396=
ENST00000307377.12:c.794G=	ENSP00000305920.8:p.Gly265=
ENST00000399402.7:c.1097G=	ENSP00000382333.2:p.Gly366=
ENST00000461475.5:n.286G=
ENST00000467571.5:n.224G=
ENST00000473477.1:n.219G=
ENST00000497796.5:n.439G=
NM_000404.2:c.1187G=	NP_000395.2:p.Gly396=
NM_000404.3:c.1187G=	NP_000395.2:p.Gly396=
NM_001079811.1:c.1097G=	NP_001073279.1:p.Gly366=
NM_001079811.2:c.1097G=	NP_001073279.1:p.Gly366=
NM_001135602.1:c.794G=	NP_001129074.1:p.Gly265=
NM_001135602.2:c.794G=	NP_001129074.1:p.Gly265=
NM_001317040.1:c.1331G=	NP_001303969.1:p.Gly444=
XR_001740634.1:n.1543-576C=
NM_000404.4:c.1187G= MANE Select	NP_000395.3:p.Gly396=
NM_001079811.3:c.1097G=	NP_001073279.2:p.Gly366=
NM_001135602.3:c.794G=	NP_001129074.2:p.Gly265=
NM_001317040.2:c.1331G=	NP_001303969.2:p.Gly444=
NM_001393580.1:c.1187G=	NP_001380509.1:p.Gly396=