Canonical Allele Identifier: CA1876865827

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962754C= , CM000671.2:g.120962754C=	GRCh38
NC_000009.11:g.123725032C= , CM000671.1:g.123725032C=	GRCh37
NC_000009.10:g.122764853C=	NCBI36
NG_007364.1:g.92523G= , LRG_28:g.92523G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1455G=
ENST00000696279.1:c.4741G=
ENST00000696280.1:n.4510G=
ENST00000696281.1:c.4439G=	ENSP00000512521.1:p.Cys1480=
ENST00000697921.1:n.3299G=
ENST00000697922.1:c.*4411G=	ENSP00000513478.1:n.*4411G=
ENST00000697923.1:n.4866G=
ENST00000223642.3:c.4421G= MANE Select	ENSP00000223642.1:p.Cys1474=
ENST00000223642.2:c.4421G=	ENSP00000223642.1:p.Cys1474=
NM_001735.2:c.4421G= , LRG_28t1:c.4421G=	NP_001726.2:p.Cys1474=
XM_011518980.1:c.4436G=	XP_011517282.1:p.Cys1479=
NM_001317163.1:c.4439G=	NP_001304092.1:p.Cys1480=
NM_001317163.2:c.4439G=	NP_001304092.1:p.Cys1480=
NM_001735.3:c.4421G= MANE Select	NP_001726.2:p.Cys1474=