Canonical Allele Identifier: CA1356010556

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33072613C= , CM000665.2:g.33072613C=	GRCh38
NC_000003.11:g.33114105C= , CM000665.1:g.33114105C=	GRCh37
NC_000003.10:g.33089109C=	NCBI36
NG_009005.1:g.29590G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.176G= MANE Select	ENSP00000306920.4:p.Arg59=
ENST00000307363.9:c.176G=	ENSP00000306920.4:p.Arg59=
ENST00000307377.12:c.176G=	ENSP00000305920.8:p.Arg59=
ENST00000399402.7:c.86G=	ENSP00000382333.2:p.Arg29=
ENST00000415454.1:c.76-14344G=	ENSP00000411813.1:n.76-14344G=
ENST00000436768.1:c.320G=	ENSP00000387989.1:p.Arg107=
ENST00000438227.1:c.76-7056G=	ENSP00000401250.1:n.76-7056G=
ENST00000440656.1:c.-148-3643G=	ENSP00000411769.1:n.-148-3643G=
ENST00000446732.5:c.86G=	ENSP00000407365.1:p.Arg29=
ENST00000450835.1:c.86G=	ENSP00000403264.1:p.Arg29=
ENST00000464355.1:n.134G=
ENST00000482097.5:n.109-19064G=
ENST00000485698.5:n.137-19064G=
ENST00000498537.5:n.133-19064G=
NM_000404.2:c.176G=	NP_000395.2:p.Arg59=
NM_000404.3:c.176G=	NP_000395.2:p.Arg59=
NM_001079811.1:c.86G=	NP_001073279.1:p.Arg29=
NM_001079811.2:c.86G=	NP_001073279.1:p.Arg29=
NM_001135602.1:c.176G=	NP_001129074.1:p.Arg59=
NM_001135602.2:c.176G=	NP_001129074.1:p.Arg59=
NM_001317040.1:c.320G=	NP_001303969.1:p.Arg107=
NM_000404.4:c.176G= MANE Select	NP_000395.3:p.Arg59=
NM_001079811.3:c.86G=	NP_001073279.2:p.Arg29=
NM_001135602.3:c.176G=	NP_001129074.2:p.Arg59=
NM_001317040.2:c.320G=	NP_001303969.2:p.Arg107=
NM_001393580.1:c.176G=	NP_001380509.1:p.Arg59=