Canonical Allele Identifier: CA1876865814

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962717C= , CM000671.2:g.120962717C=	GRCh38
NC_000009.11:g.123724995C= , CM000671.1:g.123724995C=	GRCh37
NC_000009.10:g.122764816C=	NCBI36
NG_007364.1:g.92560G= , LRG_28:g.92560G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1492G=
ENST00000696279.1:c.4778G=
ENST00000696280.1:n.4547G=
ENST00000696281.1:c.4476G=	ENSP00000512521.1:p.Gly1492=
ENST00000697921.1:n.3336G=
ENST00000697922.1:c.*4448G=	ENSP00000513478.1:n.*4448G=
ENST00000697923.1:n.4903G=
ENST00000223642.3:c.4458G= MANE Select	ENSP00000223642.1:p.Gly1486=
ENST00000223642.2:c.4458G=	ENSP00000223642.1:p.Gly1486=
NM_001735.2:c.4458G= , LRG_28t1:c.4458G=	NP_001726.2:p.Gly1486=
XM_011518980.1:c.4473G=	XP_011517282.1:p.Gly1491=
NM_001317163.1:c.4476G=	NP_001304092.1:p.Gly1492=
NM_001317163.2:c.4476G=	NP_001304092.1:p.Gly1492=
NM_001735.3:c.4458G= MANE Select	NP_001726.2:p.Gly1486=