Canonical Allele Identifier: CA1876865830

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962761A= , CM000671.2:g.120962761A=	GRCh38
NC_000009.11:g.123725039A= , CM000671.1:g.123725039A=	GRCh37
NC_000009.10:g.122764860A=	NCBI36
NG_007364.1:g.92516T= , LRG_28:g.92516T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1448T=
ENST00000696279.1:c.4734T=
ENST00000696280.1:n.4503T=
ENST00000696281.1:c.4432T=	ENSP00000512521.1:p.Phe1478=
ENST00000697921.1:n.3292T=
ENST00000697922.1:c.*4404T=	ENSP00000513478.1:n.*4404T=
ENST00000697923.1:n.4859T=
ENST00000223642.3:c.4414T= MANE Select	ENSP00000223642.1:p.Phe1472=
ENST00000223642.2:c.4414T=	ENSP00000223642.1:p.Phe1472=
NM_001735.2:c.4414T= , LRG_28t1:c.4414T=	NP_001726.2:p.Phe1472=
XM_011518980.1:c.4429T=	XP_011517282.1:p.Phe1477=
NM_001317163.1:c.4432T=	NP_001304092.1:p.Phe1478=
NM_001317163.2:c.4432T=	NP_001304092.1:p.Phe1478=
NM_001735.3:c.4414T= MANE Select	NP_001726.2:p.Phe1472=