Linked Data
MyVariant Identifiers:
chr11:g.119212387A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119341677A>G , CM000673.2:g.119341677A>G | GRCh38 |
| NC_000011.9:g.119212387A>G , CM000673.1:g.119212387A>G | GRCh37 |
| NC_000011.8:g.118717597A>G | NCBI36 |
| NG_012235.1:g.9997T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619721.6:c.1611T>C (MFRP) MANE Select | ENSP00000481824.1:p.Pro537= | |
| ENST00000360167.4:c.1257T>C (MFRP) | ENSP00000353291.4:p.Pro419= | |
| ENST00000449574.7:c.482T>C (MFRP) | ||
| ENST00000619721.5:c.1611T>C (MFRP) | ENSP00000481824.1:p.Pro537= | |
| NM_015645.4:c.-1026T>C (C1QTNF5) | NP_056460.1:n.-1026T>C | |
| NM_031433.3:c.1611T>C (MFRP) | NP_113621.1:p.Pro537= | |
| NM_031433.4:c.1611T>C (MFRP) MANE Select | NP_113621.1:p.Pro537= | |
| NM_015645.5:c.-1026T>C (C1QTNF5) | NP_056460.1:n.-1026T>C |