Canonical Allele Identifier: CA1356009057

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33068926T= , CM000665.2:g.33068926T=	GRCh38
NC_000003.11:g.33110418T= , CM000665.1:g.33110418T=	GRCh37
NC_000003.10:g.33085422T=	NCBI36
NG_009005.1:g.33277A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.290A= MANE Select	ENSP00000306920.4:p.Gln97=
ENST00000307363.9:c.290A=	ENSP00000306920.4:p.Gln97=
ENST00000307377.12:c.246-3369A=	ENSP00000305920.8:n.246-3369A=
ENST00000399402.7:c.200A=	ENSP00000382333.2:p.Gln67=
ENST00000415454.1:c.76-10657A=	ENSP00000411813.1:n.76-10657A=
ENST00000436768.1:c.434A=	ENSP00000387989.1:p.Gln145=
ENST00000438227.1:c.76-3369A=	ENSP00000401250.1:n.76-3369A=
ENST00000440656.1:c.-104A=	ENSP00000411769.1:n.-104A=
ENST00000446732.5:c.156-3369A=	ENSP00000407365.1:n.156-3369A=
ENST00000450835.1:c.200A=	ENSP00000403264.1:p.Gln67=
ENST00000464355.1:n.248A=
ENST00000482097.5:n.109-15377A=
ENST00000485698.5:n.137-15377A=
ENST00000498537.5:n.133-15377A=
NM_000404.2:c.290A=	NP_000395.2:p.Gln97=
NM_000404.3:c.290A=	NP_000395.2:p.Gln97=
NM_001079811.1:c.200A=	NP_001073279.1:p.Gln67=
NM_001079811.2:c.200A=	NP_001073279.1:p.Gln67=
NM_001135602.1:c.246-3369A=	NP_001129074.1:n.246-3369A=
NM_001135602.2:c.246-3369A=	NP_001129074.1:n.246-3369A=
NM_001317040.1:c.434A=	NP_001303969.1:p.Gln145=
NM_000404.4:c.290A= MANE Select	NP_000395.3:p.Gln97=
NM_001079811.3:c.200A=	NP_001073279.2:p.Gln67=
NM_001135602.3:c.246-3369A=	NP_001129074.2:n.246-3369A=
NM_001317040.2:c.434A=	NP_001303969.2:p.Gln145=
NM_001393580.1:c.290A=	NP_001380509.1:p.Gln97=