Canonical Allele Identifier: CA1876865905

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962956C= , CM000671.2:g.120962956C=	GRCh38
NC_000009.11:g.123725234C= , CM000671.1:g.123725234C=	GRCh37
NC_000009.10:g.122765055C=	NCBI36
NG_007364.1:g.92321G= , LRG_28:g.92321G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1369G=
ENST00000696279.1:c.4655G=
ENST00000696280.1:n.4424G=
ENST00000696281.1:c.4353G=	ENSP00000512521.1:p.Gly1451=
ENST00000697921.1:n.3213G=
ENST00000697922.1:c.*4325G=	ENSP00000513478.1:n.*4325G=
ENST00000697923.1:n.4780G=
ENST00000223642.3:c.4335G= MANE Select	ENSP00000223642.1:p.Gly1445=
ENST00000223642.2:c.4335G=	ENSP00000223642.1:p.Gly1445=
NM_001735.2:c.4335G= , LRG_28t1:c.4335G=	NP_001726.2:p.Gly1445=
XM_011518980.1:c.4350G=	XP_011517282.1:p.Gly1450=
NM_001317163.1:c.4353G=	NP_001304092.1:p.Gly1451=
NM_001317163.2:c.4353G=	NP_001304092.1:p.Gly1451=
NM_001735.3:c.4335G= MANE Select	NP_001726.2:p.Gly1445=