Canonical Allele Identifier: CA477155665
Gene: MFRP HGNC NCBI
C1QTNF5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.119215055G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119344345G>C , CM000673.2:g.119344345G>C GRCh38
NC_000011.9:g.119215055G>C , CM000673.1:g.119215055G>C GRCh37
NC_000011.8:g.118720265G>C NCBI36
NG_012235.1:g.7329C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000619721.6:c.945C>G (MFRP) MANE Select ENSP00000481824.1:p.Pro315=
ENST00000360167.4:c.898+287C>G (MFRP) ENSP00000353291.4:n.898+287C>G
ENST00000619721.5:c.945C>G (MFRP) ENSP00000481824.1:p.Pro315=
NM_015645.4:c.-1692C>G (C1QTNF5) NP_056460.1:n.-1692C>G
NM_031433.3:c.945C>G (MFRP) NP_113621.1:p.Pro315=
NM_031433.4:c.945C>G (MFRP) MANE Select NP_113621.1:p.Pro315=
NM_015645.5:c.-1692C>G (C1QTNF5) NP_056460.1:n.-1692C>G