Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.37906559_37906561delinsTCA , CM000669.2:g.37906559_37906561delinsTCA | GRCh38 |
| NC_000007.13:g.37946161_37946163delinsTCA , CM000669.1:g.37946161_37946163delinsTCA | GRCh37 |
| NC_000007.12:g.37912686_37912688delinsTCA | NCBI36 |
| NG_052980.1:g.15363_15365delinsTGA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436072.7:c.*918_*920delinsTGA (SFRP4) MANE Select | ENSP00000410715.2:n.*918_*920delinsTGA | |
| ENST00000436072.6:c.*918_*920delinsTGA (SFRP4) | ENSP00000410715.2:n.*918_*920delinsTGA | |
| ENST00000476620.1:c.-37-42281_-37-42279delinsTCA (EPDR1) | ENSP00000425858.1:n.-37-42281_-37-42279delinsTCA | |
| NM_003014.3:c.*918_*920delinsTGA (SFRP4) | NP_003005.2:n.*918_*920delinsTGA | |
| NM_003014.4:c.*918_*920delinsTGA (SFRP4) MANE Select | NP_003005.2:n.*918_*920delinsTGA |