Canonical Allele Identifier: CA1876865801

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962678G= , CM000671.2:g.120962678G=	GRCh38
NC_000009.11:g.123724956G= , CM000671.1:g.123724956G=	GRCh37
NC_000009.10:g.122764777G=	NCBI36
NG_007364.1:g.92599C= , LRG_28:g.92599C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1531C=
ENST00000696279.1:c.4817C=
ENST00000696280.1:n.4586C=
ENST00000696281.1:c.4515C=	ENSP00000512521.1:p.His1505=
ENST00000697921.1:n.3375C=
ENST00000697922.1:c.*4487C=	ENSP00000513478.1:n.*4487C=
ENST00000697923.1:n.4942C=
ENST00000223642.3:c.4497C= MANE Select	ENSP00000223642.1:p.His1499=
ENST00000223642.2:c.4497C=	ENSP00000223642.1:p.His1499=
ENST00000480188.1:n.30C=
NM_001735.2:c.4497C= , LRG_28t1:c.4497C=	NP_001726.2:p.His1499=
XM_011518980.1:c.4512C=	XP_011517282.1:p.His1504=
NM_001317163.1:c.4515C=	NP_001304092.1:p.His1505=
NM_001317163.2:c.4515C=	NP_001304092.1:p.His1505=
NM_001735.3:c.4497C= MANE Select	NP_001726.2:p.His1499=