Canonical Allele Identifier: CA1876865834

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962773G= , CM000671.2:g.120962773G=	GRCh38
NC_000009.11:g.123725051G= , CM000671.1:g.123725051G=	GRCh37
NC_000009.10:g.122764872G=	NCBI36
NG_007364.1:g.92504C= , LRG_28:g.92504C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1436C=
ENST00000696279.1:c.4722C=
ENST00000696280.1:n.4491C=
ENST00000696281.1:c.4420C=	ENSP00000512521.1:p.Pro1474=
ENST00000697921.1:n.3280C=
ENST00000697922.1:c.*4392C=	ENSP00000513478.1:n.*4392C=
ENST00000697923.1:n.4847C=
ENST00000223642.3:c.4402C= MANE Select	ENSP00000223642.1:p.Pro1468=
ENST00000223642.2:c.4402C=	ENSP00000223642.1:p.Pro1468=
NM_001735.2:c.4402C= , LRG_28t1:c.4402C=	NP_001726.2:p.Pro1468=
XM_011518980.1:c.4417C=	XP_011517282.1:p.Pro1473=
NM_001317163.1:c.4420C=	NP_001304092.1:p.Pro1474=
NM_001317163.2:c.4420C=	NP_001304092.1:p.Pro1474=
NM_001735.3:c.4402C= MANE Select	NP_001726.2:p.Pro1468=