Canonical Allele Identifier: CA1876884229

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121006746G= , CM000671.2:g.121006746G=	GRCh38
NC_000009.11:g.123769024G= , CM000671.1:g.123769024G=	GRCh37
NC_000009.10:g.122808845G=	NCBI36
NG_007364.1:g.48531C= , LRG_28:g.48531C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466280.2:c.1417+158C=	ENSP00000513491.1:n.1417+158C=
ENST00000696279.1:c.2742+158C=
ENST00000696280.1:n.2511+158C=
ENST00000696281.1:c.2440+158C=	ENSP00000512521.1:n.2440+158C=
ENST00000697921.1:n.1300+158C=
ENST00000697922.1:c.*2412+158C=	ENSP00000513478.1:n.*2412+158C=
ENST00000697923.1:n.3027+158C=
ENST00000223642.3:c.2422+158C= MANE Select	ENSP00000223642.1:n.2422+158C=
ENST00000223642.2:c.2422+158C=	ENSP00000223642.1:n.2422+158C=
ENST00000466280.1:n.25+158C=
NM_001735.2:c.2422+158C= , LRG_28t1:c.2422+158C=	NP_001726.2:n.2422+158C=
XM_011518980.1:c.2437+158C=	XP_011517282.1:n.2437+158C=
XM_011518981.1:c.2440+158C=	XP_011517283.1:n.2440+158C=
NM_001317163.1:c.2440+158C=	NP_001304092.1:n.2440+158C=
NM_001317164.1:c.2422+158C=	NP_001304093.1:n.2422+158C=
NM_001317163.2:c.2440+158C=	NP_001304092.1:n.2440+158C=
NM_001317164.2:c.2422+158C=	NP_001304093.1:n.2422+158C=
NM_001735.3:c.2422+158C= MANE Select	NP_001726.2:n.2422+158C=