Linked Data
ClinVar Variation Id:
2616
dbSNP Id:
rs104894553
ExAC:
17:3379665 G / A
gnomAD v2:
17-3379665-G-A
gnomAD v3:
17-3476371-G-A
gnomAD v4:
17-3476371-G-A
COSMIC:
COSM5566733
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.3476371G>A , CM000679.2:g.3476371G>A | GRCh38 |
| NC_000017.10:g.3379665G>A , CM000679.1:g.3379665G>A | GRCh37 |
| NC_000017.9:g.3326415G>A | NCBI36 |
| NG_008399.1:g.7262G>A | |
| NG_008399.2:g.7726G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263080.3:c.212G>A (ASPA) MANE Select | ENSP00000263080.2:p.Arg71His | |
| ENST00000263080.2:c.212G>A (ASPA) | ENSP00000263080.2:p.Arg71His | |
| ENST00000456349.6:c.212G>A (ASPA) | ENSP00000409976.2:p.Arg71His | |
| ENST00000541913.5:c.-73-6973C>T (SPATA22) | ENSP00000441920.1:n.-73-6973C>T | |
| ENST00000570318.1:c.-73-6973C>T (SPATA22) | ENSP00000459147.1:n.-73-6973C>T | |
| ENST00000571278.1:c.141+71G>A (ASPA) | ENSP00000461358.1:n.141+71G>A | |
| ENST00000577034.1:c.212G>A (ASPA) | ENSP00000458324.1:p.Arg71His | |
| NM_000049.2:c.212G>A (ASPA) | NP_000040.1:p.Arg71His | |
| NM_001128085.1:c.212G>A (ASPA) | NP_001121557.1:p.Arg71His | |
| XM_005256829.1:c.-73-6973C>T (SPATA22) | XP_005256886.1:n.-73-6973C>T | |
| XM_005256830.1:c.-73-6973C>T (SPATA22) | XP_005256887.1:n.-73-6973C>T | |
| XM_006721527.2:c.212G>A (ASPA) | XP_006721590.1:p.Arg71His | |
| XR_934026.1:n.387G>A (ASPA) | ||
| NM_001321336.1:c.-73-6973C>T (SPATA22) | NP_001308265.1:n.-73-6973C>T | |
| NM_001321337.1:c.-73-6973C>T (SPATA22) | NP_001308266.1:n.-73-6973C>T | |
| XM_017024661.1:c.212G>A (ASPA) | XP_016880150.1:p.Arg71His | |
| XM_024450764.1:c.212G>A (ASPA) | XP_024306532.1:p.Arg71His | |
| XR_934026.2:n.387G>A (ASPA) | ||
| NM_000049.3:c.212G>A (ASPA) | NP_000040.1:p.Arg71His | |
| NM_000049.4:c.212G>A (ASPA) MANE Select | NP_000040.1:p.Arg71His | |
| NM_001321336.2:c.-73-6973C>T (SPATA22) | NP_001308265.1:n.-73-6973C>T | |
| NM_001321337.2:c.-73-6973C>T (SPATA22) | NP_001308266.1:n.-73-6973C>T |