Canonical Allele Identifier: CA374746351

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123724991G>C (hg19) ; chr9:g.120962713G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962713G>C , CM000671.2:g.120962713G>C	GRCh38
NC_000009.11:g.123724991G>C , CM000671.1:g.123724991G>C	GRCh37
NC_000009.10:g.122764812G>C	NCBI36
NG_007364.1:g.92564C>G , LRG_28:g.92564C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1496C>G
ENST00000696279.1:c.4782C>G
ENST00000696280.1:n.4551C>G
ENST00000696281.1:c.4480C>G	ENSP00000512521.1:p.Leu1494Val
ENST00000697921.1:n.3340C>G
ENST00000697922.1:c.*4452C>G	ENSP00000513478.1:n.*4452C>G
ENST00000697923.1:n.4907C>G
ENST00000223642.3:c.4462C>G MANE Select	ENSP00000223642.1:p.Leu1488Val
ENST00000223642.2:c.4462C>G	ENSP00000223642.1:p.Leu1488Val
NM_001735.2:c.4462C>G , LRG_28t1:c.4462C>G	NP_001726.2:p.Leu1488Val
XM_011518980.1:c.4477C>G	XP_011517282.1:p.Leu1493Val
NM_001317163.1:c.4480C>G	NP_001304092.1:p.Leu1494Val
NM_001317163.2:c.4480C>G	NP_001304092.1:p.Leu1494Val
NM_001735.3:c.4462C>G MANE Select	NP_001726.2:p.Leu1488Val