Canonical Allele Identifier: CA1876865817

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962723T= , CM000671.2:g.120962723T=	GRCh38
NC_000009.11:g.123725001T= , CM000671.1:g.123725001T=	GRCh37
NC_000009.10:g.122764822T=	NCBI36
NG_007364.1:g.92554A= , LRG_28:g.92554A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1486A=
ENST00000696279.1:c.4772A=
ENST00000696280.1:n.4541A=
ENST00000696281.1:c.4470A=	ENSP00000512521.1:p.Glu1490=
ENST00000697921.1:n.3330A=
ENST00000697922.1:c.*4442A=	ENSP00000513478.1:n.*4442A=
ENST00000697923.1:n.4897A=
ENST00000223642.3:c.4452A= MANE Select	ENSP00000223642.1:p.Glu1484=
ENST00000223642.2:c.4452A=	ENSP00000223642.1:p.Glu1484=
NM_001735.2:c.4452A= , LRG_28t1:c.4452A=	NP_001726.2:p.Glu1484=
XM_011518980.1:c.4467A=	XP_011517282.1:p.Glu1489=
NM_001317163.1:c.4470A=	NP_001304092.1:p.Glu1490=
NM_001317163.2:c.4470A=	NP_001304092.1:p.Glu1490=
NM_001735.3:c.4452A= MANE Select	NP_001726.2:p.Glu1484=