Canonical Allele Identifier: CA2003921972
Gene: MFRP HGNC NCBI
C1QTNF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119344239A= , CM000673.2:g.119344239A= GRCh38
NC_000011.9:g.119214949A= , CM000673.1:g.119214949A= GRCh37
NC_000011.8:g.118720159A= NCBI36
NG_012235.1:g.7435T=

Transcript Alleles

HGVS Amino-acid change
ENST00000619721.6:c.975+76T= (MFRP) MANE Select ENSP00000481824.1:n.975+76T=
ENST00000360167.4:c.898+393T= (MFRP) ENSP00000353291.4:n.898+393T=
ENST00000619721.5:c.975+76T= (MFRP) ENSP00000481824.1:n.975+76T=
NM_015645.4:c.-1662+76T= (C1QTNF5) NP_056460.1:n.-1662+76T=
NM_031433.3:c.975+76T= (MFRP) NP_113621.1:n.975+76T=
NM_031433.4:c.975+76T= (MFRP) MANE Select NP_113621.1:n.975+76T=
NM_015645.5:c.-1662+76T= (C1QTNF5) NP_056460.1:n.-1662+76T=