Canonical Allele Identifier: CA382967667
Gene: C1QTNF5 HGNC NCBI
MFRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119339342C>A , CM000673.2:g.119339342C>A GRCh38
NC_000011.9:g.119210052C>A , CM000673.1:g.119210052C>A GRCh37
NC_000011.8:g.118715262C>A NCBI36
NG_012235.1:g.12332G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000528368.3:c.721G>T (C1QTNF5) MANE Select ENSP00000431140.1:p.Val241Phe
ENST00000619721.6:c.*1617G>T (MFRP) MANE Select ENSP00000481824.1:n.*1617G>T
ENST00000528368.2:c.721G>T (C1QTNF5) ENSP00000431140.1:p.Val241Phe
ENST00000530681.2:c.721G>T (C1QTNF5) ENSP00000456533.2:p.Val241Phe
ENST00000619721.5:c.*1617G>T (MFRP) ENSP00000481824.1:n.*1617G>T
NM_001278431.1:c.721G>T (C1QTNF5) NP_001265360.1:p.Val241Phe
NM_015645.4:c.721G>T (C1QTNF5) NP_056460.1:p.Val241Phe
NM_031433.3:c.*1617G>T (MFRP) NP_113621.1:n.*1617G>T
NM_001278431.2:c.721G>T (C1QTNF5) MANE Select NP_001265360.1:p.Val241Phe
NM_031433.4:c.*1617G>T (MFRP) MANE Select NP_113621.1:n.*1617G>T
NM_015645.5:c.721G>T (C1QTNF5) NP_056460.1:p.Val241Phe