Canonical Allele Identifier: CA10637995

Gene: C1QTNF5 MFRP

Linked Data

• ClinVar Variation Id: 302929
• ClinVar RCV Id: RCV000273405 ; RCV001106722
• dbSNP Id: rs886047818
• gnomAD v3: 11-119339819-G-T
• gnomAD v4: 11-119339819-G-T
• MyVariant Identifiers: chr11:g.119210529G>T (hg19) ; chr11:g.119339819G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119339819G>T , CM000673.2:g.119339819G>T	GRCh38
NC_000011.9:g.119210529G>T , CM000673.1:g.119210529G>T	GRCh37
NC_000011.8:g.118715739G>T	NCBI36
NG_012235.1:g.11855C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528368.3:c.244C>A (C1QTNF5) MANE Select	ENSP00000431140.1:p.Pro82Thr
ENST00000619721.6:c.*1140C>A (MFRP) MANE Select	ENSP00000481824.1:n.*1140C>A
ENST00000525657.2:n.134C>A (C1QTNF5)
ENST00000528368.2:c.244C>A (C1QTNF5)	ENSP00000431140.1:p.Pro82Thr
ENST00000530681.2:c.244C>A (C1QTNF5)	ENSP00000456533.2:p.Pro82Thr
ENST00000619721.5:c.*1140C>A (MFRP)	ENSP00000481824.1:n.*1140C>A
ENST00000634633.1:c.136C>A (C1QTNF5)	ENSP00000489201.1:p.Pro46Thr
NM_001278431.1:c.244C>A (C1QTNF5)	NP_001265360.1:p.Pro82Thr
NM_015645.4:c.244C>A (C1QTNF5)	NP_056460.1:p.Pro82Thr
NM_031433.3:c.*1140C>A (MFRP)	NP_113621.1:n.*1140C>A
NM_001278431.2:c.244C>A (C1QTNF5) MANE Select	NP_001265360.1:p.Pro82Thr
NM_031433.4:c.*1140C>A (MFRP) MANE Select	NP_113621.1:n.*1140C>A
NM_015645.5:c.244C>A (C1QTNF5)	NP_056460.1:p.Pro82Thr