Linked Data
MyVariant Identifiers:
chr11:g.119212449G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119341739G>T , CM000673.2:g.119341739G>T | GRCh38 |
| NC_000011.9:g.119212449G>T , CM000673.1:g.119212449G>T | GRCh37 |
| NC_000011.8:g.118717659G>T | NCBI36 |
| NG_012235.1:g.9935C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619721.6:c.1549C>A (MFRP) MANE Select | ENSP00000481824.1:p.Arg517= | |
| ENST00000360167.4:c.1195C>A (MFRP) | ENSP00000353291.4:p.Arg399= | |
| ENST00000449574.7:c.420C>A (MFRP) | ||
| ENST00000619721.5:c.1549C>A (MFRP) | ENSP00000481824.1:p.Arg517= | |
| NM_015645.4:c.-1088C>A (C1QTNF5) | NP_056460.1:n.-1088C>A | |
| NM_031433.3:c.1549C>A (MFRP) | NP_113621.1:p.Arg517= | |
| NM_031433.4:c.1549C>A (MFRP) MANE Select | NP_113621.1:p.Arg517= | |
| NM_015645.5:c.-1088C>A (C1QTNF5) | NP_056460.1:n.-1088C>A |