Linked Data
ClinVar Variation Id:
322631
ClinVar RCV Id:
RCV000276762
dbSNP Id:
rs886052821
gnomAD v2:
17-3379302-C-T
gnomAD v3:
17-3476008-C-T
gnomAD v4:
17-3476008-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.3476008C>T , CM000679.2:g.3476008C>T | GRCh38 |
| NC_000017.10:g.3379302C>T , CM000679.1:g.3379302C>T | GRCh37 |
| NC_000017.9:g.3326052C>T | NCBI36 |
| NG_008399.1:g.6899C>T | |
| NG_008399.2:g.7363C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263080.3:c.-152C>T (ASPA) MANE Select | ENSP00000263080.2:n.-152C>T | |
| ENST00000263080.2:c.-152C>T (ASPA) | ENSP00000263080.2:n.-152C>T | |
| ENST00000456349.6:c.-26-126C>T (ASPA) | ENSP00000409976.2:n.-26-126C>T | |
| ENST00000541913.5:c.-73-6610G>A (SPATA22) | ENSP00000441920.1:n.-73-6610G>A | |
| ENST00000570318.1:c.-73-6610G>A (SPATA22) | ENSP00000459147.1:n.-73-6610G>A | |
| ENST00000577034.1:c.-26-126C>T (ASPA) | ENSP00000458324.1:n.-26-126C>T | |
| NM_000049.2:c.-152C>T (ASPA) | NP_000040.1:n.-152C>T | |
| NM_001128085.1:c.-26-126C>T (ASPA) | NP_001121557.1:n.-26-126C>T | |
| XM_005256829.1:c.-73-6610G>A (SPATA22) | XP_005256886.1:n.-73-6610G>A | |
| XM_005256830.1:c.-73-6610G>A (SPATA22) | XP_005256887.1:n.-73-6610G>A | |
| XM_006721527.2:c.-26-126C>T (ASPA) | XP_006721590.1:n.-26-126C>T | |
| XR_934026.1:n.24C>T (ASPA) | ||
| NM_001321336.1:c.-73-6610G>A (SPATA22) | NP_001308265.1:n.-73-6610G>A | |
| NM_001321337.1:c.-73-6610G>A (SPATA22) | NP_001308266.1:n.-73-6610G>A | |
| XM_017024661.1:c.-26-126C>T (ASPA) | XP_016880150.1:n.-26-126C>T | |
| XM_024450764.1:c.-26-126C>T (ASPA) | XP_024306532.1:n.-26-126C>T | |
| XR_934026.2:n.24C>T (ASPA) | ||
| NM_000049.3:c.-152C>T (ASPA) | NP_000040.1:n.-152C>T | |
| NM_000049.4:c.-152C>T (ASPA) MANE Select | NP_000040.1:n.-152C>T | |
| NM_001321336.2:c.-73-6610G>A (SPATA22) | NP_001308265.1:n.-73-6610G>A | |
| NM_001321337.2:c.-73-6610G>A (SPATA22) | NP_001308266.1:n.-73-6610G>A |