Canonical Allele Identifier: CA10664548

Gene: C1QC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22645605C>T , CM000663.2:g.22645605C>T	GRCh38
NC_000001.10:g.22972098C>T , CM000663.1:g.22972098C>T	GRCh37
NC_000001.9:g.22844685C>T	NCBI36
NG_007565.1:g.6981C>T , LRG_24:g.6981C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695749.1:c.-86-1622C>T	ENSP00000512142.1:n.-86-1622C>T
ENST00000695750.1:c.181+1401C>T	ENSP00000512143.1:n.181+1401C>T
ENST00000695751.1:c.181+1401C>T	ENSP00000512144.1:n.181+1401C>T
ENST00000695752.1:c.181+1401C>T	ENSP00000512145.1:n.181+1401C>T
ENST00000695753.1:c.-86-1622C>T	ENSP00000512146.1:n.-86-1622C>T
ENST00000374640.9:c.181+1401C>T MANE Select	ENSP00000363771.4:n.181+1401C>T
ENST00000374637.1:c.181+1401C>T	ENSP00000363768.1:n.181+1401C>T
ENST00000374639.7:c.181+1401C>T	ENSP00000363770.3:n.181+1401C>T
ENST00000374640.8:c.181+1401C>T	ENSP00000363771.4:n.181+1401C>T
NM_001114101.1:c.181+1401C>T , LRG_24t1:c.181+1401C>T	NP_001107573.1:n.181+1401C>T
NM_172369.3:c.181+1401C>T	NP_758957.2:n.181+1401C>T
NM_001114101.2:c.181+1401C>T	NP_001107573.1:n.181+1401C>T
NM_001347619.1:c.181+1401C>T	NP_001334548.1:n.181+1401C>T
NM_001347620.1:c.-86-1622C>T	NP_001334549.1:n.-86-1622C>T
NM_172369.4:c.181+1401C>T	NP_758957.2:n.181+1401C>T
NM_172369.5:c.181+1401C>T MANE Select	NP_758957.2:n.181+1401C>T
NM_001114101.3:c.181+1401C>T	NP_001107573.1:n.181+1401C>T
NM_001347619.2:c.181+1401C>T	NP_001334548.1:n.181+1401C>T
NM_001347620.2:c.-86-1622C>T	NP_001334549.1:n.-86-1622C>T