Linked Data
ClinVar Variation Id:
288254
ClinVar RCV Id:
RCV000309746
RCV000313950
RCV000362228
RCV000675694
RCV001271649
RCV003930150
RCV002518027
dbSNP Id:
rs189632527
ExAC:
17:3559774 C / A
gnomAD v2:
17-3559774-C-A
gnomAD v3:
17-3656480-C-A
gnomAD v4:
17-3656480-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.3656480C>A , CM000679.2:g.3656480C>A | GRCh38 |
| NC_000017.10:g.3559774C>A , CM000679.1:g.3559774C>A | GRCh37 |
| NC_000017.9:g.3506523C>A | NCBI36 |
| NG_012489.1:g.25013C>A | |
| NG_012489.2:g.25013C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000046640.9:c.462-7C>A (CTNS) MANE Select | ENSP00000046640.4:n.462-7C>A | |
| ENST00000381870.8:c.462-7C>A (CTNS) | ENSP00000371294.3:n.462-7C>A | |
| ENST00000488623.6:c.-292-7C>A (CTNS) | ENSP00000501016.1:n.-292-7C>A | |
| ENST00000574776.6:c.21-7C>A (CTNS) | ENSP00000461118.2:n.21-7C>A | |
| ENST00000673669.1:c.21-7C>A (CTNS) | ENSP00000501123.1:n.21-7C>A | |
| ENST00000673965.1:c.462-7C>A (CTNS) | ENSP00000500995.1:n.462-7C>A | |
| ENST00000046640.7:c.462-7C>A (CTNS) | ENSP00000046640.3:n.462-7C>A | |
| ENST00000381870.7:c.462-7C>A (CTNS) | ENSP00000371294.3:n.462-7C>A | |
| ENST00000574218.1:c.21-7C>A (CTNS) | ENSP00000458912.1:n.21-7C>A | |
| ENST00000574776.5:c.21-7C>A (CTNS) | ENSP00000461118.1:n.21-7C>A | |
| ENST00000576979.1:c.462-7C>A (CTNS) | ENSP00000458457.1:n.462-7C>A | |
| NM_001031681.2:c.462-7C>A (CTNS) | NP_001026851.2:n.462-7C>A | |
| NM_004937.2:c.462-7C>A (CTNS) | NP_004928.2:n.462-7C>A | |
| XM_005256485.1:c.462-7C>A (CTNS) | XP_005256542.1:n.462-7C>A | |
| XM_006721463.1:c.462-7C>A (CTNS) | XP_006721526.1:n.462-7C>A | |
| XM_006721464.1:c.21-7C>A (CTNS) | XP_006721527.1:n.21-7C>A | |
| XM_011523691.1:c.462-7C>A (CTNS) | XP_011521993.1:n.462-7C>A | |
| XM_011523692.1:c.21-7C>A (CTNS) | XP_011521994.1:n.21-7C>A | |
| XR_934003.1:n.1055-7C>A (CTNS) | ||
| XR_934158.1:n.1143+376G>T (CTNS-AS1) | ||
| XR_934159.1:n.433+376G>T (CTNS-AS1) | ||
| XR_934160.1:n.438+376G>T (CTNS-AS1) | ||
| XR_934161.1:n.433+376G>T (CTNS-AS1) | ||
| XR_934162.1:n.438+376G>T (CTNS-AS1) | ||
| XR_934163.1:n.1034+376G>T (CTNS-AS1) | ||
| XM_005256485.3:c.462-7C>A (CTNS) | XP_005256542.1:n.462-7C>A | |
| XM_006721463.3:c.462-7C>A (CTNS) | XP_006721526.1:n.462-7C>A | |
| XM_006721464.2:c.21-7C>A (CTNS) | XP_006721527.1:n.21-7C>A | |
| XM_011523691.2:c.462-7C>A (CTNS) | XP_011521993.1:n.462-7C>A | |
| XM_011523692.2:c.21-7C>A (CTNS) | XP_011521994.1:n.21-7C>A | |
| XM_017024254.1:c.21-7C>A (CTNS) | XP_016879743.1:n.21-7C>A | |
| XM_017024255.1:c.21-7C>A (CTNS) | XP_016879744.1:n.21-7C>A | |
| XM_017024256.1:c.21-7C>A (CTNS) | XP_016879745.1:n.21-7C>A | |
| XM_017024257.1:c.21-7C>A (CTNS) | XP_016879746.1:n.21-7C>A | |
| XM_017024258.1:c.21-7C>A (CTNS) | XP_016879747.1:n.21-7C>A | |
| XR_934158.2:n.1160+376G>T (CTNS-AS1) | ||
| XR_934159.2:n.450+376G>T (CTNS-AS1) | ||
| XR_934160.2:n.455+376G>T (CTNS-AS1) | ||
| XR_934161.2:n.450+376G>T (CTNS-AS1) | ||
| XR_934162.3:n.455+376G>T (CTNS-AS1) | ||
| XR_934163.2:n.1051+376G>T (CTNS-AS1) | ||
| NM_001374492.1:c.462-7C>A (CTNS) | NP_001361421.1:n.462-7C>A | |
| NM_001374493.1:c.21-7C>A (CTNS) | NP_001361422.1:n.21-7C>A | |
| NM_001374494.1:c.21-7C>A (CTNS) | NP_001361423.1:n.21-7C>A | |
| NM_001374495.1:c.21-7C>A (CTNS) | NP_001361424.1:n.21-7C>A | |
| NM_001374496.1:c.21-7C>A (CTNS) | NP_001361425.1:n.21-7C>A | |
| NM_004937.3:c.462-7C>A (CTNS) MANE Select | NP_004928.2:n.462-7C>A | |
| NM_001031681.3:c.462-7C>A (CTNS) | NP_001026851.2:n.462-7C>A |