Canonical Allele Identifier: CA1876865842

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962805A= , CM000671.2:g.120962805A=	GRCh38
NC_000009.11:g.123725083A= , CM000671.1:g.123725083A=	GRCh37
NC_000009.10:g.122764904A=	NCBI36
NG_007364.1:g.92472T= , LRG_28:g.92472T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1433-29T=
ENST00000696279.1:c.4719-29T=
ENST00000696280.1:n.4488-29T=
ENST00000696281.1:c.4417-29T=	ENSP00000512521.1:n.4417-29T=
ENST00000697921.1:n.3277-29T=
ENST00000697922.1:c.*4389-29T=	ENSP00000513478.1:n.*4389-29T=
ENST00000697923.1:n.4844-29T=
ENST00000223642.3:c.4399-29T= MANE Select	ENSP00000223642.1:n.4399-29T=
ENST00000223642.2:c.4399-29T=	ENSP00000223642.1:n.4399-29T=
NM_001735.2:c.4399-29T= , LRG_28t1:c.4399-29T=	NP_001726.2:n.4399-29T=
XM_011518980.1:c.4414-29T=	XP_011517282.1:n.4414-29T=
NM_001317163.1:c.4417-29T=	NP_001304092.1:n.4417-29T=
NM_001317163.2:c.4417-29T=	NP_001304092.1:n.4417-29T=
NM_001735.3:c.4399-29T= MANE Select	NP_001726.2:n.4399-29T=