Canonical Allele Identifier: CA1876862486

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120954218G= , CM000671.2:g.120954218G=	GRCh38
NC_000009.11:g.123716496G= , CM000671.1:g.123716496G=	GRCh37
NC_000009.10:g.122756317G=	NCBI36
NG_007364.1:g.101059C= , LRG_28:g.101059C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.4863C=
ENST00000696279.1:c.5083-350C=
ENST00000696280.1:n.4852-350C=
ENST00000696281.1:c.4781-350C=	ENSP00000512521.1:n.4781-350C=
ENST00000697921.1:n.3641-350C=
ENST00000697922.1:c.*4753-350C=	ENSP00000513478.1:n.*4753-350C=
ENST00000697923.1:n.8274C=
ENST00000223642.3:c.4763-350C= MANE Select	ENSP00000223642.1:n.4763-350C=
ENST00000223642.2:c.4763-350C=	ENSP00000223642.1:n.4763-350C=
NM_001735.2:c.4763-350C= , LRG_28t1:c.4763-350C=	NP_001726.2:n.4763-350C=
XM_011518980.1:c.4778-350C=	XP_011517282.1:n.4778-350C=
NM_001317163.1:c.4781-350C=	NP_001304092.1:n.4781-350C=
NM_001317163.2:c.4781-350C=	NP_001304092.1:n.4781-350C=
NM_001735.3:c.4763-350C= MANE Select	NP_001726.2:n.4763-350C=