Linked Data
ClinVar Variation Id:
2166918
ClinVar RCV Id:
RCV003080324
dbSNP Id:
rs774236283
ExAC:
20:3888554 AT / A
gnomAD v2:
20-3888554-AT-A
gnomAD v4:
20-3907907-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3907912del , CM000682.2:g.3907912del | GRCh38 |
| NC_000020.10:g.3888559del , CM000682.1:g.3888559del | GRCh37 |
| NC_000020.9:g.3836559del | NCBI36 |
| NG_008131.3:g.24074del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000610179.7:c.299-14del MANE Select | ENSP00000477429.2:n.299-14del | |
| ENST00000316562.9:c.629-14del | ENSP00000313377.4:n.629-14del | |
| ENST00000336066.8:c.299-14del | ENSP00000477229.2:n.299-14del | |
| ENST00000610179.6:c.299-14del | ENSP00000477429.2:n.299-14del | |
| ENST00000643504.2:c.*72-14del | ENSP00000495157.2:n.*72-14del | |
| ENST00000646394.1:c.126-14del | ||
| ENST00000316562.8:c.629-14del | ENSP00000313377.4:n.629-14del | |
| ENST00000336066.7:c.260-14del | ENSP00000477229.1:n.260-14del | |
| ENST00000471830.1:n.173-14del | ||
| ENST00000495692.5:c.-537-14del | ENSP00000476745.1:n.-537-14del | |
| ENST00000497424.5:c.-245-14del | ENSP00000417609.1:n.-245-14del | |
| ENST00000610179.5:c.260-14del | ENSP00000477429.1:n.260-14del | |
| ENST00000621507.1:c.-245-14del | ENSP00000481523.1:n.-245-14del | |
| NM_024960.4:c.-245-14del | NP_079236.3:n.-245-14del | |
| NM_153638.2:c.629-14del | NP_705902.2:n.629-14del | |
| NM_153640.2:c.-245-14del | NP_705904.1:n.-245-14del | |
| XM_005260835.2:c.14-14del | XP_005260892.1:n.14-14del | |
| XM_005260836.3:c.-245-14del | XP_005260893.3:n.-245-14del | |
| XM_006723631.1:c.-245-14del | XP_006723694.1:n.-245-14del | |
| XM_011529364.1:c.629-14del | XP_011527666.1:n.629-14del | |
| XM_011529365.1:c.629-14del | XP_011527667.1:n.629-14del | |
| NM_001324191.1:c.-245-14del | NP_001311120.1:n.-245-14del | |
| NM_001324192.1:c.629-14del | NP_001311121.1:n.629-14del | |
| NM_001324193.1:c.-537-14del | NP_001311122.1:n.-537-14del | |
| NM_024960.5:c.-245-14del | NP_079236.3:n.-245-14del | |
| NM_153638.3:c.629-14del | NP_705902.2:n.629-14del | |
| NM_153640.3:c.-245-14del | NP_705904.1:n.-245-14del | |
| NR_136715.1:n.796-14del | ||
| XM_005260835.3:c.14-14del | XP_005260892.1:n.14-14del | |
| XM_005260836.4:c.-245-14del | XP_005260893.3:n.-245-14del | |
| XM_011529364.3:c.629-14del | XP_011527666.1:n.629-14del | |
| XM_011529365.2:c.629-14del | XP_011527667.1:n.629-14del | |
| XM_017028077.2:c.-537-14del | XP_016883566.1:n.-537-14del | |
| XM_017028078.2:c.-537-14del | XP_016883567.1:n.-537-14del | |
| XM_017028079.2:c.-537-14del | XP_016883568.1:n.-537-14del | |
| XM_024452002.1:c.-537-14del | XP_024307770.1:n.-537-14del | |
| XR_002958533.1:n.790-14del | ||
| NM_001324191.2:c.-245-14del | NP_001311120.1:n.-245-14del | |
| NM_001324193.2:c.-537-14del | NP_001311122.1:n.-537-14del | |
| NM_024960.6:c.-245-14del | NP_079236.3:n.-245-14del | |
| NR_136715.2:n.343-14del | ||
| NM_001386393.1:c.299-14del MANE Select | NP_001373322.1:n.299-14del | |
| NM_153638.4:c.629-14del | NP_705902.2:n.629-14del | |
| NM_153640.4:c.-245-14del | NP_705904.1:n.-245-14del |