Canonical Allele Identifier: CA374746687

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123725026C>G (hg19) ; chr9:g.120962748C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962748C>G , CM000671.2:g.120962748C>G	GRCh38
NC_000009.11:g.123725026C>G , CM000671.1:g.123725026C>G	GRCh37
NC_000009.10:g.122764847C>G	NCBI36
NG_007364.1:g.92529G>C , LRG_28:g.92529G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1461G>C
ENST00000696279.1:c.4747G>C
ENST00000696280.1:n.4516G>C
ENST00000696281.1:c.4445G>C	ENSP00000512521.1:p.Arg1482Pro
ENST00000697921.1:n.3305G>C
ENST00000697922.1:c.*4417G>C	ENSP00000513478.1:n.*4417G>C
ENST00000697923.1:n.4872G>C
ENST00000223642.3:c.4427G>C MANE Select	ENSP00000223642.1:p.Arg1476Pro
ENST00000223642.2:c.4427G>C	ENSP00000223642.1:p.Arg1476Pro
NM_001735.2:c.4427G>C , LRG_28t1:c.4427G>C	NP_001726.2:p.Arg1476Pro
XM_011518980.1:c.4442G>C	XP_011517282.1:p.Arg1481Pro
NM_001317163.1:c.4445G>C	NP_001304092.1:p.Arg1482Pro
NM_001317163.2:c.4445G>C	NP_001304092.1:p.Arg1482Pro
NM_001735.3:c.4427G>C MANE Select	NP_001726.2:p.Arg1476Pro