ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43091780_43091781del , CM000679.2:g.43091780_43091781del | GRCh38 |
| NC_000017.10:g.41243797_41243798del , CM000679.1:g.41243797_41243798del | GRCh37 |
| NC_000017.9:g.38497323_38497324del | NCBI36 |
| NG_005905.2:g.126205_126206del , LRG_292:g.126205_126206del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.3816_3817del | ||
| ENST00000461574.2:c.3752_3753del | ENSP00000417241.2:p.Cys1251SerfsTer3 | |
| ENST00000470026.6:c.3752_3753del | ENSP00000419274.2:p.Cys1251SerfsTer3 | |
| ENST00000473961.6:c.3626_3627del | ENSP00000420201.2:p.Cys1209SerfsTer3 | |
| ENST00000476777.6:c.3749_3750del | ENSP00000417554.2:p.Cys1250SerfsTer3 | |
| ENST00000477152.6:c.3674_3675del | ENSP00000419988.2:p.Cys1225SerfsTer3 | |
| ENST00000478531.6:c.785-747_785-746del | ENSP00000420412.2:n.785-747_785-746del | |
| ENST00000489037.2:c.3674_3675del | ENSP00000420781.2:p.Cys1225SerfsTer3 | |
| ENST00000493919.6:c.647-747_647-746del | ENSP00000418819.2:n.647-747_647-746del | |
| ENST00000494123.6:c.3752_3753del | ENSP00000419103.2:p.Cys1251SerfsTer3 | |
| ENST00000497488.2:c.2864_2865del | ENSP00000418986.2:p.Cys955SerfsTer3 | |
| ENST00000618469.2:c.3752_3753del | ENSP00000478114.2:p.Cys1251SerfsTer3 | |
| ENST00000634433.2:c.3629_3630del | ENSP00000489431.2:p.Cys1210SerfsTer3 | |
| ENST00000644379.2:c.3752_3753del | ENSP00000496570.2:p.Cys1251SerfsTer3 | |
| ENST00000644555.2:c.647-747_647-746del | ENSP00000494614.2:n.647-747_647-746del | |
| ENST00000652672.2:c.3611_3612del | ENSP00000498906.2:p.Cys1204SerfsTer3 | |
| ENST00000484087.6:c.665-747_665-746del | ENSP00000419481.2:n.665-747_665-746del | |
| ENST00000700182.1:c.707-747_707-746del | ENSP00000514849.1:n.707-747_707-746del | |
| ENST00000357654.9:c.3752_3753del MANE Select | ENSP00000350283.3:p.Cys1251SerfsTer3 | |
| ENST00000471181.7:c.3752_3753del | ENSP00000418960.2:p.Cys1251SerfsTer3 | |
| ENST00000644379.1:c.73_74del | ||
| ENST00000352993.7:c.671-747_671-746del | ENSP00000312236.5:n.671-747_671-746del | |
| ENST00000354071.7:c.3752_3753del | ENSP00000326002.7:p.Cys1251SerfsTer3 | |
| ENST00000357654.7:c.3752_3753del | ENSP00000350283.3:p.Cys1251SerfsTer3 | |
| ENST00000461221.5:c.*3535_*3536del | ENSP00000418548.1:n.*3535_*3536del | |
| ENST00000461574.1:c.46_47del | ||
| ENST00000468300.5:c.788-747_788-746del | ENSP00000417148.1:n.788-747_788-746del | |
| ENST00000471181.6:c.3752_3753del | ENSP00000418960.2:p.Cys1251SerfsTer3 | |
| ENST00000478531.5:c.785-747_785-746del | ENSP00000420412.1:n.785-747_785-746del | |
| ENST00000484087.5:c.410-747_410-746del | ENSP00000419481.1:n.410-747_410-746del | |
| ENST00000487825.5:c.413-747_413-746del | ENSP00000418212.1:n.413-747_413-746del | |
| ENST00000491747.6:c.788-747_788-746del | ENSP00000420705.2:n.788-747_788-746del | |
| ENST00000493795.5:c.3611_3612del | ENSP00000418775.1:p.Cys1204SerfsTer3 | |
| ENST00000493919.5:c.647-747_647-746del | ENSP00000418819.1:n.647-747_647-746del | |
| ENST00000586385.5:c.5-27828_5-27827del | ENSP00000465818.1:n.5-27828_5-27827del | |
| ENST00000591534.5:c.-43-17258_-43-17257del | ENSP00000467329.1:n.-43-17258_-43-17257del | |
| ENST00000591849.5:c.-99+33492_-99+33493del | ENSP00000465347.1:n.-99+33492_-99+33493del | |
| NM_007294.3:c.3752_3753del , LRG_292t1:c.3752_3753del | NP_009225.1:p.Cys1251SerfsTer3 | |
| NM_007297.3:c.3611_3612del | NP_009228.2:p.Cys1204SerfsTer3 | |
| NM_007298.3:c.788-747_788-746del | NP_009229.2:n.788-747_788-746del | |
| NM_007299.3:c.788-747_788-746del | NP_009230.2:n.788-747_788-746del | |
| NM_007300.3:c.3752_3753del | NP_009231.2:p.Cys1251SerfsTer3 | |
| NR_027676.1:n.3888_3889del | ||
| NM_007294.4:c.3752_3753del MANE Select | NP_009225.1:p.Cys1251SerfsTer3 | |
| NM_007297.4:c.3611_3612del | NP_009228.2:p.Cys1204SerfsTer3 | |
| NM_007299.4:c.788-747_788-746del | NP_009230.2:n.788-747_788-746del | |
| NM_007300.4:c.3752_3753del | NP_009231.2:p.Cys1251SerfsTer3 | |
| NR_027676.2:n.3929_3930del |