Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.37906899G>T , CM000669.2:g.37906899G>T | GRCh38 |
| NC_000007.13:g.37946501G>T , CM000669.1:g.37946501G>T | GRCh37 |
| NC_000007.12:g.37913026G>T | NCBI36 |
| NG_052980.1:g.15025C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436072.7:c.*580C>A (SFRP4) MANE Select | ENSP00000410715.2:n.*580C>A | |
| ENST00000436072.6:c.*580C>A (SFRP4) | ENSP00000410715.2:n.*580C>A | |
| ENST00000476620.1:c.-37-41941G>T (EPDR1) | ENSP00000425858.1:n.-37-41941G>T | |
| NM_003014.3:c.*580C>A (SFRP4) | NP_003005.2:n.*580C>A | |
| NM_003014.4:c.*580C>A (SFRP4) MANE Select | NP_003005.2:n.*580C>A |