gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58326988A>C , CM000679.2:g.58326988A>C | GRCh38 |
| NC_000017.10:g.56404349A>C , CM000679.1:g.56404349A>C | GRCh37 |
| NC_000017.9:g.53759348A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343736.9:c.334-198T>G (TSPOAP1) MANE Select | ENSP00000345824.4:n.334-198T>G | |
| ENST00000268893.10:c.334-198T>G (TSPOAP1) | ENSP00000268893.6:n.334-198T>G | |
| ENST00000343736.8:c.334-198T>G (TSPOAP1) | ENSP00000345824.4:n.334-198T>G | |
| NM_001261835.1:c.334-198T>G (TSPOAP1) | NP_001248764.1:n.334-198T>G | |
| NM_004758.3:c.334-198T>G (TSPOAP1) | NP_004749.2:n.334-198T>G | |
| NM_024418.2:c.334-198T>G (TSPOAP1) | NP_077729.1:n.334-198T>G | |
| NR_038410.1:n.280-1062A>C (TSPOAP1-AS1) | ||
| XM_005257807.2:c.334-198T>G (TSPOAP1) | XP_005257864.1:n.334-198T>G | |
| XM_006722173.2:c.334-198T>G (TSPOAP1) | XP_006722236.1:n.334-198T>G | |
| XM_006722174.2:c.334-198T>G (TSPOAP1) | XP_006722237.1:n.334-198T>G | |
| XM_006722175.2:c.334-198T>G (TSPOAP1) | XP_006722238.1:n.334-198T>G | |
| XM_006722176.2:c.334-198T>G (TSPOAP1) | XP_006722239.1:n.334-198T>G | |
| XR_934597.1:n.1209-198T>G (TSPOAP1) | ||
| XR_934598.1:n.1209-198T>G (TSPOAP1) | ||
| XR_934599.1:n.1209-198T>G (TSPOAP1) | ||
| XM_005257807.3:c.334-198T>G (TSPOAP1) | XP_005257864.1:n.334-198T>G | |
| XM_006722173.3:c.334-198T>G (TSPOAP1) | XP_006722236.1:n.334-198T>G | |
| XM_006722174.3:c.334-198T>G (TSPOAP1) | XP_006722237.1:n.334-198T>G | |
| XM_006722175.3:c.334-198T>G (TSPOAP1) | XP_006722238.1:n.334-198T>G | |
| XM_006722176.3:c.334-198T>G (TSPOAP1) | XP_006722239.1:n.334-198T>G | |
| XM_017025326.2:c.334-198T>G (TSPOAP1) | XP_016880815.1:n.334-198T>G | |
| XM_017025327.1:c.217-198T>G (TSPOAP1) | XP_016880816.1:n.217-198T>G | |
| XM_017025328.2:c.334-198T>G (TSPOAP1) | XP_016880817.1:n.334-198T>G | |
| XM_017025329.2:c.334-198T>G (TSPOAP1) | XP_016880818.1:n.334-198T>G | |
| XM_017025330.2:c.334-198T>G (TSPOAP1) | XP_016880819.1:n.334-198T>G | |
| XM_017025331.2:c.334-198T>G (TSPOAP1) | XP_016880820.1:n.334-198T>G | |
| XM_017025332.2:c.334-198T>G (TSPOAP1) | XP_016880821.1:n.334-198T>G | |
| XM_017025333.2:c.334-198T>G (TSPOAP1) | XP_016880822.1:n.334-198T>G | |
| XM_017025334.2:c.334-198T>G (TSPOAP1) | XP_016880823.1:n.334-198T>G | |
| XR_002958085.1:n.1444-198T>G (TSPOAP1) | ||
| XR_934597.2:n.1444-198T>G (TSPOAP1) | ||
| NM_004758.4:c.334-198T>G (TSPOAP1) MANE Select | NP_004749.2:n.334-198T>G | |
| NM_001261835.2:c.334-198T>G (TSPOAP1) | NP_001248764.1:n.334-198T>G | |
| NM_024418.3:c.334-198T>G (TSPOAP1) | NP_077729.1:n.334-198T>G |