Canonical Allele Identifier: CA2785814118

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120954185C>A , CM000671.2:g.120954185C>A	GRCh38
NC_000009.11:g.123716463C>A , CM000671.1:g.123716463C>A	GRCh37
NC_000009.10:g.122756284C>A	NCBI36
NG_007364.1:g.101092G>T , LRG_28:g.101092G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.4896G>T
ENST00000696279.1:c.5083-317G>T
ENST00000696280.1:n.4852-317G>T
ENST00000696281.1:c.4781-317G>T	ENSP00000512521.1:n.4781-317G>T
ENST00000697921.1:n.3641-317G>T
ENST00000697922.1:c.*4753-317G>T	ENSP00000513478.1:n.*4753-317G>T
ENST00000697923.1:n.8307G>T
ENST00000223642.3:c.4763-317G>T MANE Select	ENSP00000223642.1:n.4763-317G>T
ENST00000223642.2:c.4763-317G>T	ENSP00000223642.1:n.4763-317G>T
NM_001735.2:c.4763-317G>T , LRG_28t1:c.4763-317G>T	NP_001726.2:n.4763-317G>T
XM_011518980.1:c.4778-317G>T	XP_011517282.1:n.4778-317G>T
NM_001317163.1:c.4781-317G>T	NP_001304092.1:n.4781-317G>T
NM_001317163.2:c.4781-317G>T	NP_001304092.1:n.4781-317G>T
NM_001735.3:c.4763-317G>T MANE Select	NP_001726.2:n.4763-317G>T