Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.37906902T>A , CM000669.2:g.37906902T>A | GRCh38 |
| NC_000007.13:g.37946504T>A , CM000669.1:g.37946504T>A | GRCh37 |
| NC_000007.12:g.37913029T>A | NCBI36 |
| NG_052980.1:g.15022A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436072.7:c.*577A>T (SFRP4) MANE Select | ENSP00000410715.2:n.*577A>T | |
| ENST00000436072.6:c.*577A>T (SFRP4) | ENSP00000410715.2:n.*577A>T | |
| ENST00000476620.1:c.-37-41938T>A (EPDR1) | ENSP00000425858.1:n.-37-41938T>A | |
| NM_003014.3:c.*577A>T (SFRP4) | NP_003005.2:n.*577A>T | |
| NM_003014.4:c.*577A>T (SFRP4) MANE Select | NP_003005.2:n.*577A>T |