Canonical Allele Identifier: CA1876862469

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120954163C= , CM000671.2:g.120954163C=	GRCh38
NC_000009.11:g.123716441C= , CM000671.1:g.123716441C=	GRCh37
NC_000009.10:g.122756262C=	NCBI36
NG_007364.1:g.101114G= , LRG_28:g.101114G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.4918G=
ENST00000696279.1:c.5083-295G=
ENST00000696280.1:n.4852-295G=
ENST00000696281.1:c.4781-295G=	ENSP00000512521.1:n.4781-295G=
ENST00000697921.1:n.3641-295G=
ENST00000697922.1:c.*4753-295G=	ENSP00000513478.1:n.*4753-295G=
ENST00000697923.1:n.8329G=
ENST00000223642.3:c.4763-295G= MANE Select	ENSP00000223642.1:n.4763-295G=
ENST00000223642.2:c.4763-295G=	ENSP00000223642.1:n.4763-295G=
NM_001735.2:c.4763-295G= , LRG_28t1:c.4763-295G=	NP_001726.2:n.4763-295G=
XM_011518980.1:c.4778-295G=	XP_011517282.1:n.4778-295G=
NM_001317163.1:c.4781-295G=	NP_001304092.1:n.4781-295G=
NM_001317163.2:c.4781-295G=	NP_001304092.1:n.4781-295G=
NM_001735.3:c.4763-295G= MANE Select	NP_001726.2:n.4763-295G=