Canonical Allele Identifier: CA1356000965

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33051791A= , CM000665.2:g.33051791A=	GRCh38
NC_000003.11:g.33093283A= , CM000665.1:g.33093283A=	GRCh37
NC_000003.10:g.33068287A=	NCBI36
NG_009005.1:g.50412T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.922T= MANE Select	NP_000395.3:p.Phe308=
ENST00000307363.10:c.922T= MANE Select	ENSP00000306920.4:p.Phe308=
NM_000404.2:c.922T=	NP_000395.2:p.Phe308=
NM_000404.3:c.922T=	NP_000395.2:p.Phe308=
NM_001079811.1:c.832T=	NP_001073279.1:p.Phe278=
NM_001079811.2:c.832T=	NP_001073279.1:p.Phe278=
NM_001079811.3:c.832T=	NP_001073279.2:p.Phe278=
NM_001135602.1:c.529T=	NP_001129074.1:p.Phe177=
NM_001135602.2:c.529T=	NP_001129074.1:p.Phe177=
NM_001135602.3:c.529T=	NP_001129074.2:p.Phe177=
NM_001317040.1:c.1066T=	NP_001303969.1:p.Phe356=
NM_001317040.2:c.1066T=	NP_001303969.2:p.Phe356=
NM_001393580.1:c.922T=	NP_001380509.1:p.Phe308=
ENST00000307363.9:c.922T=	ENSP00000306920.4:p.Phe308=
ENST00000307377.12:c.529T=	ENSP00000305920.8:p.Phe177=
ENST00000399402.7:c.832T=	ENSP00000382333.2:p.Phe278=
ENST00000415454.1:c.445T=	ENSP00000411813.1:p.Phe149=
ENST00000482097.5:n.297T=
ENST00000485698.5:n.325T=
ENST00000498537.5:n.448T=