Canonical Allele Identifier: CA1876865851

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962824T= , CM000671.2:g.120962824T=	GRCh38
NC_000009.11:g.123725102T= , CM000671.1:g.123725102T=	GRCh37
NC_000009.10:g.122764923T=	NCBI36
NG_007364.1:g.92453A= , LRG_28:g.92453A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1433-48A=
ENST00000696279.1:c.4719-48A=
ENST00000696280.1:n.4488-48A=
ENST00000696281.1:c.4417-48A=	ENSP00000512521.1:n.4417-48A=
ENST00000697921.1:n.3277-48A=
ENST00000697922.1:c.*4389-48A=	ENSP00000513478.1:n.*4389-48A=
ENST00000697923.1:n.4844-48A=
ENST00000223642.3:c.4399-48A= MANE Select	ENSP00000223642.1:n.4399-48A=
ENST00000223642.2:c.4399-48A=	ENSP00000223642.1:n.4399-48A=
NM_001735.2:c.4399-48A= , LRG_28t1:c.4399-48A=	NP_001726.2:n.4399-48A=
XM_011518980.1:c.4414-48A=	XP_011517282.1:n.4414-48A=
NM_001317163.1:c.4417-48A=	NP_001304092.1:n.4417-48A=
NM_001317163.2:c.4417-48A=	NP_001304092.1:n.4417-48A=
NM_001735.3:c.4399-48A= MANE Select	NP_001726.2:n.4399-48A=