Canonical Allele Identifier: CA338932982

Gene: C1QC

Linked Data

• MyVariant Identifiers: chr1:g.22970616G>C (hg19) ; chr1:g.22644123G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22644123G>C , CM000663.2:g.22644123G>C	GRCh38
NC_000001.10:g.22970616G>C , CM000663.1:g.22970616G>C	GRCh37
NC_000001.9:g.22843203G>C	NCBI36
NG_007565.1:g.5499G>C , LRG_24:g.5499G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695749.1:c.-87+409G>C	ENSP00000512142.1:n.-87+409G>C
ENST00000695750.1:c.100G>C	ENSP00000512143.1:p.Gly34Arg
ENST00000695751.1:c.100G>C	ENSP00000512144.1:p.Gly34Arg
ENST00000695752.1:c.100G>C	ENSP00000512145.1:p.Gly34Arg
ENST00000695753.1:c.-87+237G>C	ENSP00000512146.1:n.-87+237G>C
ENST00000374640.9:c.100G>C MANE Select	ENSP00000363771.4:p.Gly34Arg
ENST00000374637.1:c.100G>C	ENSP00000363768.1:p.Gly34Arg
ENST00000374639.7:c.100G>C	ENSP00000363770.3:p.Gly34Arg
ENST00000374640.8:c.100G>C	ENSP00000363771.4:p.Gly34Arg
NM_001114101.1:c.100G>C , LRG_24t1:c.100G>C	NP_001107573.1:p.Gly34Arg
NM_172369.3:c.100G>C	NP_758957.2:p.Gly34Arg
NM_001114101.2:c.100G>C	NP_001107573.1:p.Gly34Arg
NM_001347619.1:c.100G>C	NP_001334548.1:p.Gly34Arg
NM_001347620.1:c.-87+409G>C	NP_001334549.1:n.-87+409G>C
NM_172369.4:c.100G>C	NP_758957.2:p.Gly34Arg
NM_172369.5:c.100G>C MANE Select	NP_758957.2:p.Gly34Arg
NM_001114101.3:c.100G>C	NP_001107573.1:p.Gly34Arg
NM_001347619.2:c.100G>C	NP_001334548.1:p.Gly34Arg
NM_001347620.2:c.-87+409G>C	NP_001334549.1:n.-87+409G>C