Canonical Allele Identifier: CA1876865807

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962692C= , CM000671.2:g.120962692C=	GRCh38
NC_000009.11:g.123724970C= , CM000671.1:g.123724970C=	GRCh37
NC_000009.10:g.122764791C=	NCBI36
NG_007364.1:g.92585G= , LRG_28:g.92585G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1517G=
ENST00000696279.1:c.4803G=
ENST00000696280.1:n.4572G=
ENST00000696281.1:c.4501G=	ENSP00000512521.1:p.Val1501=
ENST00000697921.1:n.3361G=
ENST00000697922.1:c.*4473G=	ENSP00000513478.1:n.*4473G=
ENST00000697923.1:n.4928G=
ENST00000223642.3:c.4483G= MANE Select	ENSP00000223642.1:p.Val1495=
ENST00000223642.2:c.4483G=	ENSP00000223642.1:p.Val1495=
ENST00000480188.1:n.16G=
NM_001735.2:c.4483G= , LRG_28t1:c.4483G=	NP_001726.2:p.Val1495=
XM_011518980.1:c.4498G=	XP_011517282.1:p.Val1500=
NM_001317163.1:c.4501G=	NP_001304092.1:p.Val1501=
NM_001317163.2:c.4501G=	NP_001304092.1:p.Val1501=
NM_001735.3:c.4483G= MANE Select	NP_001726.2:p.Val1495=