Canonical Allele Identifier: CA374746942

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123725050G>C (hg19) ; chr9:g.120962772G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962772G>C , CM000671.2:g.120962772G>C	GRCh38
NC_000009.11:g.123725050G>C , CM000671.1:g.123725050G>C	GRCh37
NC_000009.10:g.122764871G>C	NCBI36
NG_007364.1:g.92505C>G , LRG_28:g.92505C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1437C>G
ENST00000696279.1:c.4723C>G
ENST00000696280.1:n.4492C>G
ENST00000696281.1:c.4421C>G	ENSP00000512521.1:p.Pro1474Arg
ENST00000697921.1:n.3281C>G
ENST00000697922.1:c.*4393C>G	ENSP00000513478.1:n.*4393C>G
ENST00000697923.1:n.4848C>G
ENST00000223642.3:c.4403C>G MANE Select	ENSP00000223642.1:p.Pro1468Arg
ENST00000223642.2:c.4403C>G	ENSP00000223642.1:p.Pro1468Arg
NM_001735.2:c.4403C>G , LRG_28t1:c.4403C>G	NP_001726.2:p.Pro1468Arg
XM_011518980.1:c.4418C>G	XP_011517282.1:p.Pro1473Arg
NM_001317163.1:c.4421C>G	NP_001304092.1:p.Pro1474Arg
NM_001317163.2:c.4421C>G	NP_001304092.1:p.Pro1474Arg
NM_001735.3:c.4403C>G MANE Select	NP_001726.2:p.Pro1468Arg