Canonical Allele Identifier: CA1876865800

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962672T= , CM000671.2:g.120962672T=	GRCh38
NC_000009.11:g.123724950T= , CM000671.1:g.123724950T=	GRCh37
NC_000009.10:g.122764771T=	NCBI36
NG_007364.1:g.92605A= , LRG_28:g.92605A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1537A=
ENST00000696279.1:c.4823A=
ENST00000696280.1:n.4592A=
ENST00000696281.1:c.4521A=	ENSP00000512521.1:p.Pro1507=
ENST00000697921.1:n.3381A=
ENST00000697922.1:c.*4493A=	ENSP00000513478.1:n.*4493A=
ENST00000697923.1:n.4948A=
ENST00000223642.3:c.4503A= MANE Select	ENSP00000223642.1:p.Pro1501=
ENST00000223642.2:c.4503A=	ENSP00000223642.1:p.Pro1501=
ENST00000480188.1:n.36A=
NM_001735.2:c.4503A= , LRG_28t1:c.4503A=	NP_001726.2:p.Pro1501=
XM_011518980.1:c.4518A=	XP_011517282.1:p.Pro1506=
NM_001317163.1:c.4521A=	NP_001304092.1:p.Pro1507=
NM_001317163.2:c.4521A=	NP_001304092.1:p.Pro1507=
NM_001735.3:c.4503A= MANE Select	NP_001726.2:p.Pro1501=