Linked Data
ClinVar Variation Id:
1072306
dbSNP Id:
rs1328663348
gnomAD v2:
20-35559210-TCACTTATCTG-T
gnomAD v3:
20-36930807-TCACTTATCTG-T
gnomAD v4:
20-36930807-TCACTTATCTG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.36930810_36930819del , CM000682.2:g.36930810_36930819del | GRCh38 |
| NC_000020.10:g.35559213_35559222del , CM000682.1:g.35559213_35559222del | GRCh37 |
| NC_000020.9:g.34992627_34992636del | NCBI36 |
| NG_017059.1:g.26027_26036del , LRG_281:g.26027_26036del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644114.2:c.568_577del | ENSP00000494354.2:p.Gln190AsnfsTer? | |
| ENST00000644250.2:c.568_577del | ENSP00000493810.2:p.Gln190AsnfsTer? | |
| ENST00000644688.2:n.630_639del | ||
| ENST00000645444.2:c.568_577del | ENSP00000495381.2:p.Gln190AsnfsTer? | |
| ENST00000682773.1:c.568_577del | ENSP00000507178.1:p.Gln190AsnfsTer? | |
| ENST00000683720.1:c.568_577del | ENSP00000508219.1:p.Gln190AsnfsTer? | |
| ENST00000683766.1:c.568_577del | ENSP00000506877.1:p.Gln190AsnfsTer? | |
| ENST00000262878.5:c.568_577del | ENSP00000262878.5:p.Gln190AsnfsTer? | |
| ENST00000642186.1:c.568_577del | ENSP00000494436.1:p.Gln190AsnfsTer? | |
| ENST00000642246.1:c.*247_*256del | ENSP00000494979.1:n.*247_*256del | |
| ENST00000642616.1:c.*45_*54del | ENSP00000494271.1:n.*45_*54del | |
| ENST00000643078.1:c.*247_*256del | ENSP00000496474.1:n.*247_*256del | |
| ENST00000643161.1:n.131_140del | ||
| ENST00000643918.1:c.568_577del | ENSP00000493928.1:p.Gln190AsnfsTer? | |
| ENST00000644114.1:c.494_503del | ||
| ENST00000644370.1:n.509_518del | ||
| ENST00000645033.1:c.568_577del | ENSP00000494520.1:p.Gln190AsnfsTer? | |
| ENST00000645444.1:c.336_345del | ||
| ENST00000646066.1:c.568_577del | ENSP00000495432.1:p.Gln190AsnfsTer? | |
| ENST00000646121.1:c.285_294del | ||
| ENST00000646673.2:c.568_577del MANE Select | ENSP00000493536.2:p.Gln190AsnfsTer? | |
| ENST00000646866.1:c.*17_*26del | ENSP00000495737.1:n.*17_*26del | |
| ENST00000646869.1:c.568_577del | ENSP00000495667.1:p.Gln190AsnfsTer? | |
| ENST00000646904.1:c.568_577del | ENSP00000494823.1:p.Gln190AsnfsTer? | |
| ENST00000647095.1:n.639_648del | ||
| ENST00000647163.1:c.568_577del | ENSP00000494313.1:p.Gln190AsnfsTer? | |
| ENST00000647459.1:n.595_604del | ||
| ENST00000262878.4:c.568_577del | ENSP00000262878.4:p.Gln190AsnfsTer? | |
| NM_015474.3:c.568_577del , LRG_281t1:c.568_577del | NP_056289.2:p.Gln190AsnfsTer? | |
| XM_005260384.2:c.568_577del | XP_005260441.1:p.Gln190AsnfsTer? | |
| XM_011528761.1:c.568_577del | XP_011527063.1:p.Gln190AsnfsTer? | |
| NM_001363729.1:c.568_577del | NP_001350658.1:p.Gln190AsnfsTer? | |
| NM_001363733.1:c.568_577del | NP_001350662.1:p.Gln190AsnfsTer? | |
| NM_001363729.2:c.568_577del | NP_001350658.1:p.Gln190AsnfsTer? | |
| NM_001363733.2:c.568_577del | NP_001350662.1:p.Gln190AsnfsTer? | |
| NM_015474.4:c.568_577del MANE Select | NP_056289.2:p.Gln190AsnfsTer? |