Canonical Allele Identifier: CA374746533

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123725009G>C (hg19) ; chr9:g.120962731G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962731G>C , CM000671.2:g.120962731G>C	GRCh38
NC_000009.11:g.123725009G>C , CM000671.1:g.123725009G>C	GRCh37
NC_000009.10:g.122764830G>C	NCBI36
NG_007364.1:g.92546C>G , LRG_28:g.92546C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1478C>G
ENST00000696279.1:c.4764C>G
ENST00000696280.1:n.4533C>G
ENST00000696281.1:c.4462C>G	ENSP00000512521.1:p.Leu1488Val
ENST00000697921.1:n.3322C>G
ENST00000697922.1:c.*4434C>G	ENSP00000513478.1:n.*4434C>G
ENST00000697923.1:n.4889C>G
ENST00000223642.3:c.4444C>G MANE Select	ENSP00000223642.1:p.Leu1482Val
ENST00000223642.2:c.4444C>G	ENSP00000223642.1:p.Leu1482Val
NM_001735.2:c.4444C>G , LRG_28t1:c.4444C>G	NP_001726.2:p.Leu1482Val
XM_011518980.1:c.4459C>G	XP_011517282.1:p.Leu1487Val
NM_001317163.1:c.4462C>G	NP_001304092.1:p.Leu1488Val
NM_001317163.2:c.4462C>G	NP_001304092.1:p.Leu1488Val
NM_001735.3:c.4444C>G MANE Select	NP_001726.2:p.Leu1482Val