Canonical Allele Identifier: CA1876868326

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120968960A= , CM000671.2:g.120968960A=	GRCh38
NC_000009.11:g.123731238A= , CM000671.1:g.123731238A=	GRCh37
NC_000009.10:g.122771059A=	NCBI36
NG_007364.1:g.86317T= , LRG_28:g.86317T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1254+101T=
ENST00000696279.1:c.4540+101T=
ENST00000696280.1:n.4309+101T=
ENST00000696281.1:c.4238+101T=	ENSP00000512521.1:n.4238+101T=
ENST00000697921.1:n.3098+101T=
ENST00000697922.1:c.*4210+101T=	ENSP00000513478.1:n.*4210+101T=
ENST00000697923.1:n.4665+101T=
ENST00000223642.3:c.4220+101T= MANE Select	ENSP00000223642.1:n.4220+101T=
ENST00000223642.2:c.4220+101T=	ENSP00000223642.1:n.4220+101T=
NM_001735.2:c.4220+101T= , LRG_28t1:c.4220+101T=	NP_001726.2:n.4220+101T=
XM_011518980.1:c.4235+101T=	XP_011517282.1:n.4235+101T=
NM_001317163.1:c.4238+101T=	NP_001304092.1:n.4238+101T=
NM_001317163.2:c.4238+101T=	NP_001304092.1:n.4238+101T=
NM_001735.3:c.4220+101T= MANE Select	NP_001726.2:n.4220+101T=