Linked Data
ClinVar Variation Id:
2606
ClinVar RCV Id:
RCV000002724
dbSNP Id:
rs104894548
PubMed:
PMID:7599639
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.3483520T>C , CM000679.2:g.3483520T>C | GRCh38 |
| NC_000017.10:g.3386814T>C , CM000679.1:g.3386814T>C | GRCh37 |
| NC_000017.9:g.3333564T>C | NCBI36 |
| NG_008399.1:g.14411T>C | |
| NG_008399.2:g.14875T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000263080.3:c.454T>C (ASPA) MANE Select | ENSP00000263080.2:p.Cys152Arg | |
| ENST00000263080.2:c.454T>C (ASPA) | ENSP00000263080.2:p.Cys152Arg | |
| ENST00000456349.6:c.454T>C (ASPA) | ENSP00000409976.2:p.Cys152Arg | |
| ENST00000541913.5:c.-73-14122A>G (SPATA22) | ENSP00000441920.1:n.-73-14122A>G | |
| ENST00000570318.1:c.-73-14122A>G (SPATA22) | ENSP00000459147.1:n.-73-14122A>G | |
| ENST00000571278.1:c.*188T>C (ASPA) | ENSP00000461358.1:n.*188T>C | |
| NM_000049.2:c.454T>C (ASPA) | NP_000040.1:p.Cys152Arg | |
| NM_001128085.1:c.454T>C (ASPA) | NP_001121557.1:p.Cys152Arg | |
| XM_005256829.1:c.-73-14122A>G (SPATA22) | XP_005256886.1:n.-73-14122A>G | |
| XM_005256830.1:c.-73-14122A>G (SPATA22) | XP_005256887.1:n.-73-14122A>G | |
| XM_006721527.2:c.454T>C (ASPA) | XP_006721590.1:p.Cys152Arg | |
| XR_934026.1:n.629T>C (ASPA) | ||
| NM_001321336.1:c.-73-14122A>G (SPATA22) | NP_001308265.1:n.-73-14122A>G | |
| NM_001321337.1:c.-73-14122A>G (SPATA22) | NP_001308266.1:n.-73-14122A>G | |
| XM_017024661.1:c.454T>C (ASPA) | XP_016880150.1:p.Cys152Arg | |
| XM_024450764.1:c.454T>C (ASPA) | XP_024306532.1:p.Cys152Arg | |
| XR_934026.2:n.629T>C (ASPA) | ||
| NM_000049.3:c.454T>C (ASPA) | NP_000040.1:p.Cys152Arg | |
| NM_000049.4:c.454T>C (ASPA) MANE Select | NP_000040.1:p.Cys152Arg | |
| NM_001321336.2:c.-73-14122A>G (SPATA22) | NP_001308265.1:n.-73-14122A>G | |
| NM_001321337.2:c.-73-14122A>G (SPATA22) | NP_001308266.1:n.-73-14122A>G |