Linked Data
gnomAD v4:
11-119341702-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119341702G>T , CM000673.2:g.119341702G>T | GRCh38 |
| NC_000011.9:g.119212412G>T , CM000673.1:g.119212412G>T | GRCh37 |
| NC_000011.8:g.118717622G>T | NCBI36 |
| NG_012235.1:g.9972C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619721.6:c.1586C>A (MFRP) MANE Select | ENSP00000481824.1:p.Thr529Asn | |
| ENST00000360167.4:c.1232C>A (MFRP) | ENSP00000353291.4:p.Thr411Asn | |
| ENST00000449574.7:c.457C>A (MFRP) | ||
| ENST00000619721.5:c.1586C>A (MFRP) | ENSP00000481824.1:p.Thr529Asn | |
| NM_015645.4:c.-1051C>A (C1QTNF5) | NP_056460.1:n.-1051C>A | |
| NM_031433.3:c.1586C>A (MFRP) | NP_113621.1:p.Thr529Asn | |
| NM_031433.4:c.1586C>A (MFRP) MANE Select | NP_113621.1:p.Thr529Asn | |
| NM_015645.5:c.-1051C>A (C1QTNF5) | NP_056460.1:n.-1051C>A |