Canonical Allele Identifier: CA1356003838

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33058221G= , CM000665.2:g.33058221G=	GRCh38
NC_000003.11:g.33099713G= , CM000665.1:g.33099713G=	GRCh37
NC_000003.10:g.33074717G=	NCBI36
NG_009005.1:g.43982C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.601C= MANE Select	NP_000395.3:p.Arg201=
ENST00000307363.10:c.601C= MANE Select	ENSP00000306920.4:p.Arg201=
NM_000404.2:c.601C=	NP_000395.2:p.Arg201=
NM_000404.3:c.601C=	NP_000395.2:p.Arg201=
NM_001079811.1:c.511C=	NP_001073279.1:p.Arg171=
NM_001079811.2:c.511C=	NP_001073279.1:p.Arg171=
NM_001079811.3:c.511C=	NP_001073279.2:p.Arg171=
NM_001135602.1:c.341-4672C=	NP_001129074.1:n.341-4672C=
NM_001135602.2:c.341-4672C=	NP_001129074.1:n.341-4672C=
NM_001135602.3:c.341-4672C=	NP_001129074.2:n.341-4672C=
NM_001317040.1:c.745C=	NP_001303969.1:p.Arg249=
NM_001317040.2:c.745C=	NP_001303969.2:p.Arg249=
NM_001393580.1:c.601C=	NP_001380509.1:p.Arg201=
ENST00000307363.9:c.601C=	ENSP00000306920.4:p.Arg201=
ENST00000307377.12:c.341-4672C=	ENSP00000305920.8:n.341-4672C=
ENST00000399402.7:c.511C=	ENSP00000382333.2:p.Arg171=
ENST00000415454.1:c.124C=	ENSP00000411813.1:p.Arg42=
ENST00000438227.1:c.*93C=	ENSP00000401250.1:n.*93C=
ENST00000440656.1:c.208C=	ENSP00000411769.1:p.Arg70=
ENST00000446732.5:c.*44C=	ENSP00000407365.1:n.*44C=
ENST00000482097.5:n.109-4672C=
ENST00000485698.5:n.137-4672C=
ENST00000498537.5:n.133-4672C=