Canonical Allele Identifier: CA382978386
Gene: MFRP HGNC NCBI
C1QTNF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119345569G>C , CM000673.2:g.119345569G>C GRCh38
NC_000011.9:g.119216279G>C , CM000673.1:g.119216279G>C GRCh37
NC_000011.8:g.118721489G>C NCBI36
NG_012235.1:g.6105C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000619721.6:c.492C>G (MFRP) MANE Select ENSP00000481824.1:p.Tyr164Ter
ENST00000360167.4:c.492C>G (MFRP) ENSP00000353291.4:p.Tyr164Ter
ENST00000529147.2:n.455C>G (MFRP)
ENST00000619721.5:c.492C>G (MFRP) ENSP00000481824.1:p.Tyr164Ter
ENST00000634542.1:c.*83C>G (MFRP) ENSP00000488979.1:n.*83C>G
NM_015645.4:c.-2145C>G (C1QTNF5) NP_056460.1:n.-2145C>G
NM_031433.3:c.492C>G (MFRP) NP_113621.1:p.Tyr164Ter
NM_031433.4:c.492C>G (MFRP) MANE Select NP_113621.1:p.Tyr164Ter
NM_015645.5:c.-2145C>G (C1QTNF5) NP_056460.1:n.-2145C>G