Canonical Allele Identifier: CA1876862468

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120954161A= , CM000671.2:g.120954161A=	GRCh38
NC_000009.11:g.123716439A= , CM000671.1:g.123716439A=	GRCh37
NC_000009.10:g.122756260A=	NCBI36
NG_007364.1:g.101116T= , LRG_28:g.101116T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.4920T=
ENST00000696279.1:c.5083-293T=
ENST00000696280.1:n.4852-293T=
ENST00000696281.1:c.4781-293T=	ENSP00000512521.1:n.4781-293T=
ENST00000697921.1:n.3641-293T=
ENST00000697922.1:c.*4753-293T=	ENSP00000513478.1:n.*4753-293T=
ENST00000697923.1:n.8331T=
ENST00000223642.3:c.4763-293T= MANE Select	ENSP00000223642.1:n.4763-293T=
ENST00000223642.2:c.4763-293T=	ENSP00000223642.1:n.4763-293T=
NM_001735.2:c.4763-293T= , LRG_28t1:c.4763-293T=	NP_001726.2:n.4763-293T=
XM_011518980.1:c.4778-293T=	XP_011517282.1:n.4778-293T=
NM_001317163.1:c.4781-293T=	NP_001304092.1:n.4781-293T=
NM_001317163.2:c.4781-293T=	NP_001304092.1:n.4781-293T=
NM_001735.3:c.4763-293T= MANE Select	NP_001726.2:n.4763-293T=