ClinVar RCV:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.119245796C>A , CM000664.2:g.119245796C>A | GRCh38 |
| NC_000002.11:g.120003372C>A , CM000664.1:g.120003372C>A | GRCh37 |
| NC_000002.10:g.119719842C>A | NCBI36 |
| NG_042823.1:g.26989C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393110.7:c.330C>A (STEAP3) MANE Select | ENSP00000376822.2:p.Cys110Ter | |
| ENST00000393106.6:c.300C>A (STEAP3) | ENSP00000376818.2:p.Cys100Ter | |
| ENST00000393107.2:c.300C>A (STEAP3) | ENSP00000376819.2:p.Cys100Ter | |
| ENST00000393110.6:c.330C>A (STEAP3) | ENSP00000376822.2:p.Cys110Ter | |
| ENST00000409811.5:c.300C>A (STEAP3) | ENSP00000386510.1:p.Cys100Ter | |
| NM_001008410.1:c.300C>A (STEAP3) | NP_001008410.1:p.Cys100Ter | |
| NM_018234.2:c.300C>A (STEAP3) | NP_060704.2:p.Cys100Ter | |
| NM_138637.2:c.300C>A (STEAP3) | NP_619543.2:p.Cys100Ter | |
| NM_182915.2:c.330C>A (STEAP3) | NP_878919.2:p.Cys110Ter | |
| NR_046721.1:n.1844G>T (STEAP3-AS1) | ||
| XM_006712614.2:c.300C>A (STEAP3) | XP_006712677.1:p.Cys100Ter | |
| XM_006712615.1:c.300C>A (STEAP3) | XP_006712678.1:p.Cys100Ter | |
| XM_011511403.1:c.300C>A (STEAP3) | XP_011509705.1:p.Cys100Ter | |
| XM_006712614.3:c.300C>A (STEAP3) | XP_006712677.1:p.Cys100Ter | |
| NM_182915.3:c.330C>A (STEAP3) MANE Select | NP_878919.2:p.Cys110Ter | |
| NM_001008410.2:c.300C>A (STEAP3) | NP_001008410.1:p.Cys100Ter | |
| NM_018234.3:c.300C>A (STEAP3) | NP_060704.2:p.Cys100Ter | |
| NM_138637.3:c.300C>A (STEAP3) | NP_619543.2:p.Cys100Ter |