Canonical Allele Identifier: CA1356001062

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33051979C= , CM000665.2:g.33051979C=	GRCh38
NC_000003.11:g.33093471C= , CM000665.1:g.33093471C=	GRCh37
NC_000003.10:g.33068475C=	NCBI36
NG_009005.1:g.50224G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.818G= MANE Select	NP_000395.3:p.Trp273=
ENST00000307363.10:c.818G= MANE Select	ENSP00000306920.4:p.Trp273=
NM_000404.2:c.818G=	NP_000395.2:p.Trp273=
NM_000404.3:c.818G=	NP_000395.2:p.Trp273=
NM_001079811.1:c.728G=	NP_001073279.1:p.Trp243=
NM_001079811.2:c.728G=	NP_001073279.1:p.Trp243=
NM_001079811.3:c.728G=	NP_001073279.2:p.Trp243=
NM_001135602.1:c.425G=	NP_001129074.1:p.Trp142=
NM_001135602.2:c.425G=	NP_001129074.1:p.Trp142=
NM_001135602.3:c.425G=	NP_001129074.2:p.Trp142=
NM_001317040.1:c.962G=	NP_001303969.1:p.Trp321=
NM_001317040.2:c.962G=	NP_001303969.2:p.Trp321=
NM_001393580.1:c.818G=	NP_001380509.1:p.Trp273=
ENST00000307363.9:c.818G=	ENSP00000306920.4:p.Trp273=
ENST00000307377.12:c.425G=	ENSP00000305920.8:p.Trp142=
ENST00000399402.7:c.728G=	ENSP00000382333.2:p.Trp243=
ENST00000415454.1:c.341G=	ENSP00000411813.1:p.Trp114=
ENST00000438227.1:c.*310G=	ENSP00000401250.1:n.*310G=
ENST00000446732.5:c.*261G=	ENSP00000407365.1:n.*261G=
ENST00000482097.5:n.193G=
ENST00000485698.5:n.221G=
ENST00000498537.5:n.344G=