Canonical Allele Identifier: CA2616410047
Gene: MFRP HGNC NCBI
C1QTNF5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119344269G>A , CM000673.2:g.119344269G>A GRCh38
NC_000011.9:g.119214979G>A , CM000673.1:g.119214979G>A GRCh37
NC_000011.8:g.118720189G>A NCBI36
NG_012235.1:g.7405C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000619721.6:c.975+46C>T (MFRP) MANE Select ENSP00000481824.1:n.975+46C>T
ENST00000360167.4:c.898+363C>T (MFRP) ENSP00000353291.4:n.898+363C>T
ENST00000619721.5:c.975+46C>T (MFRP) ENSP00000481824.1:n.975+46C>T
NM_015645.4:c.-1662+46C>T (C1QTNF5) NP_056460.1:n.-1662+46C>T
NM_031433.3:c.975+46C>T (MFRP) NP_113621.1:n.975+46C>T
NM_031433.4:c.975+46C>T (MFRP) MANE Select NP_113621.1:n.975+46C>T
NM_015645.5:c.-1662+46C>T (C1QTNF5) NP_056460.1:n.-1662+46C>T