Canonical Allele Identifier: CA1876865913

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962974G= , CM000671.2:g.120962974G=	GRCh38
NC_000009.11:g.123725252G= , CM000671.1:g.123725252G=	GRCh37
NC_000009.10:g.122765073G=	NCBI36
NG_007364.1:g.92303C= , LRG_28:g.92303C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1358-7C=
ENST00000696279.1:c.4644-7C=
ENST00000696280.1:n.4413-7C=
ENST00000696281.1:c.4342-7C=	ENSP00000512521.1:n.4342-7C=
ENST00000697921.1:n.3202-7C=
ENST00000697922.1:c.*4314-7C=	ENSP00000513478.1:n.*4314-7C=
ENST00000697923.1:n.4769-7C=
ENST00000223642.3:c.4324-7C= MANE Select	ENSP00000223642.1:n.4324-7C=
ENST00000223642.2:c.4324-7C=	ENSP00000223642.1:n.4324-7C=
NM_001735.2:c.4324-7C= , LRG_28t1:c.4324-7C=	NP_001726.2:n.4324-7C=
XM_011518980.1:c.4339-7C=	XP_011517282.1:n.4339-7C=
NM_001317163.1:c.4342-7C=	NP_001304092.1:n.4342-7C=
NM_001317163.2:c.4342-7C=	NP_001304092.1:n.4342-7C=
NM_001735.3:c.4324-7C= MANE Select	NP_001726.2:n.4324-7C=