Canonical Allele Identifier: CA1876865896

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962934A= , CM000671.2:g.120962934A=	GRCh38
NC_000009.11:g.123725212A= , CM000671.1:g.123725212A=	GRCh37
NC_000009.10:g.122765033A=	NCBI36
NG_007364.1:g.92343T= , LRG_28:g.92343T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1391T=
ENST00000696279.1:c.4677T=
ENST00000696280.1:n.4446T=
ENST00000696281.1:c.4375T=	ENSP00000512521.1:p.Tyr1459=
ENST00000697921.1:n.3235T=
ENST00000697922.1:c.*4347T=	ENSP00000513478.1:n.*4347T=
ENST00000697923.1:n.4802T=
ENST00000223642.3:c.4357T= MANE Select	ENSP00000223642.1:p.Tyr1453=
ENST00000223642.2:c.4357T=	ENSP00000223642.1:p.Tyr1453=
NM_001735.2:c.4357T= , LRG_28t1:c.4357T=	NP_001726.2:p.Tyr1453=
XM_011518980.1:c.4372T=	XP_011517282.1:p.Tyr1458=
NM_001317163.1:c.4375T=	NP_001304092.1:p.Tyr1459=
NM_001317163.2:c.4375T=	NP_001304092.1:p.Tyr1459=
NM_001735.3:c.4357T= MANE Select	NP_001726.2:p.Tyr1453=