Canonical Allele Identifier: CA1876865819

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962732T= , CM000671.2:g.120962732T=	GRCh38
NC_000009.11:g.123725010T= , CM000671.1:g.123725010T=	GRCh37
NC_000009.10:g.122764831T=	NCBI36
NG_007364.1:g.92545A= , LRG_28:g.92545A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1477A=
ENST00000696279.1:c.4763A=
ENST00000696280.1:n.4532A=
ENST00000696281.1:c.4461A=	ENSP00000512521.1:p.Glu1487=
ENST00000697921.1:n.3321A=
ENST00000697922.1:c.*4433A=	ENSP00000513478.1:n.*4433A=
ENST00000697923.1:n.4888A=
ENST00000223642.3:c.4443A= MANE Select	ENSP00000223642.1:p.Glu1481=
ENST00000223642.2:c.4443A=	ENSP00000223642.1:p.Glu1481=
NM_001735.2:c.4443A= , LRG_28t1:c.4443A=	NP_001726.2:p.Glu1481=
XM_011518980.1:c.4458A=	XP_011517282.1:p.Glu1486=
NM_001317163.1:c.4461A=	NP_001304092.1:p.Glu1487=
NM_001317163.2:c.4461A=	NP_001304092.1:p.Glu1487=
NM_001735.3:c.4443A= MANE Select	NP_001726.2:p.Glu1481=