Canonical Allele Identifier: CA1876865893

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962928T= , CM000671.2:g.120962928T=	GRCh38
NC_000009.11:g.123725206T= , CM000671.1:g.123725206T=	GRCh37
NC_000009.10:g.122765027T=	NCBI36
NG_007364.1:g.92349A= , LRG_28:g.92349A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1397A=
ENST00000696279.1:c.4683A=
ENST00000696280.1:n.4452A=
ENST00000696281.1:c.4381A=	ENSP00000512521.1:p.Ile1461=
ENST00000697921.1:n.3241A=
ENST00000697922.1:c.*4353A=	ENSP00000513478.1:n.*4353A=
ENST00000697923.1:n.4808A=
ENST00000223642.3:c.4363A= MANE Select	ENSP00000223642.1:p.Ile1455=
ENST00000223642.2:c.4363A=	ENSP00000223642.1:p.Ile1455=
NM_001735.2:c.4363A= , LRG_28t1:c.4363A=	NP_001726.2:p.Ile1455=
XM_011518980.1:c.4378A=	XP_011517282.1:p.Ile1460=
NM_001317163.1:c.4381A=	NP_001304092.1:p.Ile1461=
NM_001317163.2:c.4381A=	NP_001304092.1:p.Ile1461=
NM_001735.3:c.4363A= MANE Select	NP_001726.2:p.Ile1455=