Canonical Allele Identifier: CA477155671
Gene: MFRP HGNC NCBI
C1QTNF5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.119215061A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119344351A>G , CM000673.2:g.119344351A>G GRCh38
NC_000011.9:g.119215061A>G , CM000673.1:g.119215061A>G GRCh37
NC_000011.8:g.118720271A>G NCBI36
NG_012235.1:g.7323T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000619721.6:c.939T>C (MFRP) MANE Select ENSP00000481824.1:p.Ser313=
ENST00000360167.4:c.898+281T>C (MFRP) ENSP00000353291.4:n.898+281T>C
ENST00000619721.5:c.939T>C (MFRP) ENSP00000481824.1:p.Ser313=
NM_015645.4:c.-1698T>C (C1QTNF5) NP_056460.1:n.-1698T>C
NM_031433.3:c.939T>C (MFRP) NP_113621.1:p.Ser313=
NM_031433.4:c.939T>C (MFRP) MANE Select NP_113621.1:p.Ser313=
NM_015645.5:c.-1698T>C (C1QTNF5) NP_056460.1:n.-1698T>C