Canonical Allele Identifier: CA1876874348

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120980439T= , CM000671.2:g.120980439T=	GRCh38
NC_000009.11:g.123742717T= , CM000671.1:g.123742717T=	GRCh37
NC_000009.10:g.122782538T=	NCBI36
NG_007364.1:g.74838A= , LRG_28:g.74838A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000480188.2:n.398-185A=
ENST00000696279.1:c.3807-185A=
ENST00000696280.1:n.3576-185A=
ENST00000696281.1:c.3505-185A=	ENSP00000512521.1:n.3505-185A=
ENST00000697921.1:n.2365-185A=
ENST00000697922.1:c.*3477-185A=	ENSP00000513478.1:n.*3477-185A=
ENST00000697923.1:n.3932-185A=
ENST00000223642.3:c.3487-185A= MANE Select	ENSP00000223642.1:n.3487-185A=
ENST00000223642.2:c.3487-185A=	ENSP00000223642.1:n.3487-185A=
ENST00000489802.1:n.50-185A=
NM_001735.2:c.3487-185A= , LRG_28t1:c.3487-185A=	NP_001726.2:n.3487-185A=
XM_011518980.1:c.3502-185A=	XP_011517282.1:n.3502-185A=
NM_001317163.1:c.3505-185A=	NP_001304092.1:n.3505-185A=
NM_001317163.2:c.3505-185A=	NP_001304092.1:n.3505-185A=
NM_001735.3:c.3487-185A= MANE Select	NP_001726.2:n.3487-185A=