Canonical Allele Identifier: CA6320609
Community Standard Title: NM_031433.4(MFRP):c.335C>T (p.Thr112Met)
Gene: MFRP HGNC NCBI
C1QTNF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119345865G>A , CM000673.2:g.119345865G>A GRCh38
NC_000011.9:g.119216575G>A , CM000673.1:g.119216575G>A GRCh37
NC_000011.8:g.118721785G>A NCBI36
NG_012235.1:g.5809C>T

Transcript Alleles

HGVS Amino-acid Change
NM_031433.4:c.335C>T (MFRP) MANE Select NP_113621.1:p.Thr112Met
ENST00000619721.6:c.335C>T (MFRP) MANE Select ENSP00000481824.1:p.Thr112Met
NM_015645.4:c.-2302C>T (C1QTNF5) NP_056460.1:n.-2302C>T
NM_015645.5:c.-2302C>T (C1QTNF5) NP_056460.1:n.-2302C>T
NM_031433.3:c.335C>T (MFRP) NP_113621.1:p.Thr112Met
ENST00000360167.4:c.335C>T (MFRP) ENSP00000353291.4:p.Thr112Met
ENST00000526059.1:n.493C>T (MFRP)
ENST00000529147.2:n.298C>T (MFRP)
ENST00000619721.5:c.335C>T (MFRP) ENSP00000481824.1:p.Thr112Met
ENST00000634542.1:c.232C>T (MFRP) ENSP00000488979.1:p.Arg78Ter