Canonical Allele Identifier: CA1355998428

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33046184G= , CM000665.2:g.33046184G=	GRCh38
NC_000003.11:g.33087676G= , CM000665.1:g.33087676G=	GRCh37
NC_000003.10:g.33062680G=	NCBI36
NG_009005.1:g.56019C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.1004C= MANE Select	NP_000395.3:p.Ala335=
ENST00000307363.10:c.1004C= MANE Select	ENSP00000306920.4:p.Ala335=
NM_000404.2:c.1004C=	NP_000395.2:p.Ala335=
NM_000404.3:c.1004C=	NP_000395.2:p.Ala335=
NM_001079811.1:c.914C=	NP_001073279.1:p.Ala305=
NM_001079811.2:c.914C=	NP_001073279.1:p.Ala305=
NM_001079811.3:c.914C=	NP_001073279.2:p.Ala305=
NM_001135602.1:c.611C=	NP_001129074.1:p.Ala204=
NM_001135602.2:c.611C=	NP_001129074.1:p.Ala204=
NM_001135602.3:c.611C=	NP_001129074.2:p.Ala204=
NM_001317040.1:c.1148C=	NP_001303969.1:p.Ala383=
NM_001317040.2:c.1148C=	NP_001303969.2:p.Ala383=
NM_001393580.1:c.1004C=	NP_001380509.1:p.Ala335=
ENST00000307363.9:c.1004C=	ENSP00000306920.4:p.Ala335=
ENST00000307377.12:c.611C=	ENSP00000305920.8:p.Ala204=
ENST00000399402.7:c.914C=	ENSP00000382333.2:p.Ala305=
ENST00000415454.1:c.527C=	ENSP00000411813.1:p.Ala176=
ENST00000482097.5:n.379C=
ENST00000485698.5:n.407C=
ENST00000490658.2:n.9C=
ENST00000498537.5:n.530C=