Canonical Allele Identifier: CA1356000954

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33051766T= , CM000665.2:g.33051766T=	GRCh38
NC_000003.11:g.33093258T= , CM000665.1:g.33093258T=	GRCh37
NC_000003.10:g.33068262T=	NCBI36
NG_009005.1:g.50437A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.947A= MANE Select	ENSP00000306920.4:p.Tyr316=
ENST00000307363.9:c.947A=	ENSP00000306920.4:p.Tyr316=
ENST00000307377.12:c.554A=	ENSP00000305920.8:p.Tyr185=
ENST00000399402.7:c.857A=	ENSP00000382333.2:p.Tyr286=
ENST00000415454.1:c.470A=	ENSP00000411813.1:p.Tyr157=
ENST00000482097.5:n.322A=
ENST00000485698.5:n.350A=
ENST00000498537.5:n.473A=
NM_000404.2:c.947A=	NP_000395.2:p.Tyr316=
NM_000404.3:c.947A=	NP_000395.2:p.Tyr316=
NM_001079811.1:c.857A=	NP_001073279.1:p.Tyr286=
NM_001079811.2:c.857A=	NP_001073279.1:p.Tyr286=
NM_001135602.1:c.554A=	NP_001129074.1:p.Tyr185=
NM_001135602.2:c.554A=	NP_001129074.1:p.Tyr185=
NM_001317040.1:c.1091A=	NP_001303969.1:p.Tyr364=
NM_000404.4:c.947A= MANE Select	NP_000395.3:p.Tyr316=
NM_001079811.3:c.857A=	NP_001073279.2:p.Tyr286=
NM_001135602.3:c.554A=	NP_001129074.2:p.Tyr185=
NM_001317040.2:c.1091A=	NP_001303969.2:p.Tyr364=
NM_001393580.1:c.947A=	NP_001380509.1:p.Tyr316=