Canonical Allele Identifier: CA1876865724

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962472G= , CM000671.2:g.120962472G=	GRCh38
NC_000009.11:g.123724750G= , CM000671.1:g.123724750G=	GRCh37
NC_000009.10:g.122764571G=	NCBI36
NG_007364.1:g.92805C= , LRG_28:g.92805C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1538+199C=
ENST00000696279.1:c.4824+199C=
ENST00000696280.1:n.4593+199C=
ENST00000696281.1:c.4522+199C=	ENSP00000512521.1:n.4522+199C=
ENST00000697921.1:n.3382+199C=
ENST00000697922.1:c.*4494+199C=	ENSP00000513478.1:n.*4494+199C=
ENST00000697923.1:n.4949+199C=
ENST00000223642.3:c.4504+199C= MANE Select	ENSP00000223642.1:n.4504+199C=
ENST00000223642.2:c.4504+199C=	ENSP00000223642.1:n.4504+199C=
ENST00000480188.1:n.37+199C=
NM_001735.2:c.4504+199C= , LRG_28t1:c.4504+199C=	NP_001726.2:n.4504+199C=
XM_011518980.1:c.4519+199C=	XP_011517282.1:n.4519+199C=
NM_001317163.1:c.4522+199C=	NP_001304092.1:n.4522+199C=
NM_001317163.2:c.4522+199C=	NP_001304092.1:n.4522+199C=
NM_001735.3:c.4504+199C= MANE Select	NP_001726.2:n.4504+199C=