Canonical Allele Identifier: CA1355984364

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33014263C= , CM000665.2:g.33014263C=	GRCh38
NC_000003.11:g.33055755C= , CM000665.1:g.33055755C=	GRCh37
NC_000003.10:g.33030759C=	NCBI36
NG_009005.1:g.87940G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.1527G= MANE Select	NP_000395.3:p.Trp509=
ENST00000307363.10:c.1527G= MANE Select	ENSP00000306920.4:p.Trp509=
NM_000404.2:c.1527G=	NP_000395.2:p.Trp509=
NM_000404.3:c.1527G=	NP_000395.2:p.Trp509=
NM_001079811.1:c.1437G=	NP_001073279.1:p.Trp479=
NM_001079811.2:c.1437G=	NP_001073279.1:p.Trp479=
NM_001079811.3:c.1437G=	NP_001073279.2:p.Trp479=
NM_001135602.1:c.1134G=	NP_001129074.1:p.Trp378=
NM_001135602.2:c.1134G=	NP_001129074.1:p.Trp378=
NM_001135602.3:c.1134G=	NP_001129074.2:p.Trp378=
NM_001317040.1:c.1671G=	NP_001303969.1:p.Trp557=
NM_001317040.2:c.1671G=	NP_001303969.2:p.Trp557=
NM_001393580.1:c.1527G=	NP_001380509.1:p.Trp509=
ENST00000307363.9:c.1527G=	ENSP00000306920.4:p.Trp509=
ENST00000307377.12:c.1134G=	ENSP00000305920.8:p.Trp378=
ENST00000399402.7:c.1437G=	ENSP00000382333.2:p.Trp479=
ENST00000461475.5:n.626G=
ENST00000497796.5:n.779G=