Canonical Allele Identifier: CA1876880146

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120997683C= , CM000671.2:g.120997683C=	GRCh38
NC_000009.11:g.123759961C= , CM000671.1:g.123759961C=	GRCh37
NC_000009.10:g.122799782C=	NCBI36
NG_007364.1:g.57594G= , LRG_28:g.57594G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001735.3:c.2654G= MANE Select	NP_001726.2:p.Arg885=
ENST00000223642.3:c.2654G= MANE Select	ENSP00000223642.1:p.Arg885=
NM_001317163.1:c.2672G=	NP_001304092.1:p.Arg891=
NM_001317163.2:c.2672G=	NP_001304092.1:p.Arg891=
NM_001735.2:c.2654G= , LRG_28t1:c.2654G=	NP_001726.2:p.Arg885=
ENST00000223642.2:c.2654G=	ENSP00000223642.1:p.Arg885=
ENST00000696279.1:c.2974G=
ENST00000696280.1:n.2743G=
ENST00000696281.1:c.2672G=	ENSP00000512521.1:p.Arg891=
ENST00000697921.1:n.1532G=
ENST00000697922.1:c.*2644G=	ENSP00000513478.1:n.*2644G=
ENST00000697923.1:n.3259G=
XM_011518980.1:c.2669G=	XP_011517282.1:p.Arg890=
XM_011518981.1:c.2672G=	XP_011517283.1:p.Arg891=