Canonical Allele Identifier: CA1876868359

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120969033A= , CM000671.2:g.120969033A=	GRCh38
NC_000009.11:g.123731311A= , CM000671.1:g.123731311A=	GRCh37
NC_000009.10:g.122771132A=	NCBI36
NG_007364.1:g.86244T= , LRG_28:g.86244T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000480188.2:n.1254+28T=
ENST00000696279.1:c.4540+28T=
ENST00000696280.1:n.4309+28T=
ENST00000696281.1:c.4238+28T=	ENSP00000512521.1:n.4238+28T=
ENST00000697921.1:n.3098+28T=
ENST00000697922.1:c.*4210+28T=	ENSP00000513478.1:n.*4210+28T=
ENST00000697923.1:n.4665+28T=
ENST00000223642.3:c.4220+28T= MANE Select	ENSP00000223642.1:n.4220+28T=
ENST00000223642.2:c.4220+28T=	ENSP00000223642.1:n.4220+28T=
NM_001735.2:c.4220+28T= , LRG_28t1:c.4220+28T=	NP_001726.2:n.4220+28T=
XM_011518980.1:c.4235+28T=	XP_011517282.1:n.4235+28T=
NM_001317163.1:c.4238+28T=	NP_001304092.1:n.4238+28T=
NM_001317163.2:c.4238+28T=	NP_001304092.1:n.4238+28T=
NM_001735.3:c.4220+28T= MANE Select	NP_001726.2:n.4220+28T=