Canonical Allele Identifier: CA2003917464
Gene: MFRP HGNC NCBI
C1QTNF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119341577C= , CM000673.2:g.119341577C= GRCh38
NC_000011.9:g.119212287C= , CM000673.1:g.119212287C= GRCh37
NC_000011.8:g.118717497C= NCBI36
NG_012235.1:g.10097G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000619721.6:c.1711G= (MFRP) MANE Select ENSP00000481824.1:p.Ala571=
ENST00000360167.4:c.1357G= (MFRP) ENSP00000353291.4:p.Ala453=
ENST00000619721.5:c.1711G= (MFRP) ENSP00000481824.1:p.Ala571=
NM_015645.4:c.-926G= (C1QTNF5) NP_056460.1:n.-926G=
NM_031433.3:c.1711G= (MFRP) NP_113621.1:p.Ala571=
NM_031433.4:c.1711G= (MFRP) MANE Select NP_113621.1:p.Ala571=
NM_015645.5:c.-926G= (C1QTNF5) NP_056460.1:n.-926G=