Canonical Allele Identifier: CA1355987539

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33021647T= , CM000665.2:g.33021647T=	GRCh38
NC_000003.11:g.33063139T= , CM000665.1:g.33063139T=	GRCh37
NC_000003.10:g.33038143T=	NCBI36
NG_009005.1:g.80556A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1152A= MANE Select	ENSP00000306920.4:p.Thr384=
ENST00000307363.9:c.1152A=	ENSP00000306920.4:p.Thr384=
ENST00000307377.12:c.759A=	ENSP00000305920.8:p.Thr253=
ENST00000399402.7:c.1062A=	ENSP00000382333.2:p.Thr354=
ENST00000461475.5:n.251A=
ENST00000467571.5:n.189A=
ENST00000473477.1:n.184A=
ENST00000482097.5:n.527A=
ENST00000497796.5:n.404A=
NM_000404.2:c.1152A=	NP_000395.2:p.Thr384=
NM_000404.3:c.1152A=	NP_000395.2:p.Thr384=
NM_001079811.1:c.1062A=	NP_001073279.1:p.Thr354=
NM_001079811.2:c.1062A=	NP_001073279.1:p.Thr354=
NM_001135602.1:c.759A=	NP_001129074.1:p.Thr253=
NM_001135602.2:c.759A=	NP_001129074.1:p.Thr253=
NM_001317040.1:c.1296A=	NP_001303969.1:p.Thr432=
XR_001740634.1:n.1543-541T=
NM_000404.4:c.1152A= MANE Select	NP_000395.3:p.Thr384=
NM_001079811.3:c.1062A=	NP_001073279.2:p.Thr354=
NM_001135602.3:c.759A=	NP_001129074.2:p.Thr253=
NM_001317040.2:c.1296A=	NP_001303969.2:p.Thr432=
NM_001393580.1:c.1152A=	NP_001380509.1:p.Thr384=