Canonical Allele Identifier: CA1876865835

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962775A= , CM000671.2:g.120962775A=	GRCh38
NC_000009.11:g.123725053A= , CM000671.1:g.123725053A=	GRCh37
NC_000009.10:g.122764874A=	NCBI36
NG_007364.1:g.92502T= , LRG_28:g.92502T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1434T=
ENST00000696279.1:c.4720T=
ENST00000696280.1:n.4489T=
ENST00000696281.1:c.4418T=	ENSP00000512521.1:p.Ile1473=
ENST00000697921.1:n.3278T=
ENST00000697922.1:c.*4390T=	ENSP00000513478.1:n.*4390T=
ENST00000697923.1:n.4845T=
ENST00000223642.3:c.4400T= MANE Select	ENSP00000223642.1:p.Ile1467=
ENST00000223642.2:c.4400T=	ENSP00000223642.1:p.Ile1467=
NM_001735.2:c.4400T= , LRG_28t1:c.4400T=	NP_001726.2:p.Ile1467=
XM_011518980.1:c.4415T=	XP_011517282.1:p.Ile1472=
NM_001317163.1:c.4418T=	NP_001304092.1:p.Ile1473=
NM_001317163.2:c.4418T=	NP_001304092.1:p.Ile1473=
NM_001735.3:c.4400T= MANE Select	NP_001726.2:p.Ile1467=