ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43094549_43094550del , CM000679.2:g.43094549_43094550del | GRCh38 |
| NC_000017.10:g.41246566_41246567del , CM000679.1:g.41246566_41246567del | GRCh37 |
| NC_000017.9:g.38500092_38500093del | NCBI36 |
| NG_005905.2:g.123434_123435del , LRG_292:g.123434_123435del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.1045_1046del | ||
| ENST00000461574.2:c.981_982del | ENSP00000417241.2:p.Cys328Ter | |
| ENST00000470026.6:c.981_982del | ENSP00000419274.2:p.Cys328Ter | |
| ENST00000473961.6:c.855_856del | ENSP00000420201.2:p.Cys286Ter | |
| ENST00000476777.6:c.978_979del | ENSP00000417554.2:p.Cys327Ter | |
| ENST00000477152.6:c.903_904del | ENSP00000419988.2:p.Cys302Ter | |
| ENST00000478531.6:c.784+194_784+195del | ENSP00000420412.2:n.784+194_784+195del | |
| ENST00000489037.2:c.903_904del | ENSP00000420781.2:p.Cys302Ter | |
| ENST00000493919.6:c.646+194_646+195del | ENSP00000418819.2:n.646+194_646+195del | |
| ENST00000494123.6:c.981_982del | ENSP00000419103.2:p.Cys328Ter | |
| ENST00000497488.2:c.93_94del | ENSP00000418986.2:p.Cys32Ter | |
| ENST00000618469.2:c.981_982del | ENSP00000478114.2:p.Cys328Ter | |
| ENST00000634433.2:c.858_859del | ENSP00000489431.2:p.Cys287Ter | |
| ENST00000644379.2:c.981_982del | ENSP00000496570.2:p.Cys328Ter | |
| ENST00000644555.2:c.646+194_646+195del | ENSP00000494614.2:n.646+194_646+195del | |
| ENST00000652672.2:c.840_841del | ENSP00000498906.2:p.Cys281Ter | |
| ENST00000484087.6:c.664+194_664+195del | ENSP00000419481.2:n.664+194_664+195del | |
| ENST00000700182.1:c.706+194_706+195del | ENSP00000514849.1:n.706+194_706+195del | |
| ENST00000700183.1:c.*989_*990del | ENSP00000514850.1:n.*989_*990del | |
| ENST00000357654.9:c.981_982del MANE Select | ENSP00000350283.3:p.Cys328Ter | |
| ENST00000471181.7:c.981_982del | ENSP00000418960.2:p.Cys328Ter | |
| ENST00000642945.1:c.*855_*856del | ENSP00000495897.1:n.*855_*856del | |
| ENST00000652672.1:c.840_841del | ENSP00000498906.1:p.Cys281Ter | |
| ENST00000352993.7:c.670+1296_670+1297del | ENSP00000312236.5:n.670+1296_670+1297del | |
| ENST00000354071.7:c.981_982del | ENSP00000326002.7:p.Cys328Ter | |
| ENST00000357654.7:c.981_982del | ENSP00000350283.3:p.Cys328Ter | |
| ENST00000412061.3:c.332_333del | ||
| ENST00000461221.5:c.*764_*765del | ENSP00000418548.1:n.*764_*765del | |
| ENST00000468300.5:c.787+194_787+195del | ENSP00000417148.1:n.787+194_787+195del | |
| ENST00000470026.5:c.981_982del | ENSP00000419274.1:p.Cys328Ter | |
| ENST00000471181.6:c.981_982del | ENSP00000418960.2:p.Cys328Ter | |
| ENST00000473961.5:c.578_579del | ||
| ENST00000477152.5:c.903_904del | ENSP00000419988.1:p.Cys302Ter | |
| ENST00000478531.5:c.784+194_784+195del | ENSP00000420412.1:n.784+194_784+195del | |
| ENST00000484087.5:c.409+194_409+195del | ENSP00000419481.1:n.409+194_409+195del | |
| ENST00000487825.5:c.412+194_412+195del | ENSP00000418212.1:n.412+194_412+195del | |
| ENST00000491747.6:c.787+194_787+195del | ENSP00000420705.2:n.787+194_787+195del | |
| ENST00000492859.5:c.*917_*918del | ENSP00000420253.1:n.*917_*918del | |
| ENST00000493795.5:c.840_841del | ENSP00000418775.1:p.Cys281Ter | |
| ENST00000493919.5:c.646+194_646+195del | ENSP00000418819.1:n.646+194_646+195del | |
| ENST00000494123.5:c.981_982del | ENSP00000419103.1:p.Cys328Ter | |
| ENST00000497488.1:c.93_94del | ENSP00000418986.1:p.Cys32Ter | |
| ENST00000586385.5:c.5-30599_5-30598del | ENSP00000465818.1:n.5-30599_5-30598del | |
| ENST00000591534.5:c.-43-20029_-43-20028del | ENSP00000467329.1:n.-43-20029_-43-20028del | |
| ENST00000591849.5:c.-99+30721_-99+30722del | ENSP00000465347.1:n.-99+30721_-99+30722del | |
| ENST00000634433.1:c.858_859del | ENSP00000489431.1:p.Cys287Ter | |
| NM_007294.3:c.981_982del , LRG_292t1:c.981_982del | NP_009225.1:p.Cys328Ter | |
| NM_007297.3:c.840_841del | NP_009228.2:p.Cys281Ter | |
| NM_007298.3:c.787+194_787+195del | NP_009229.2:n.787+194_787+195del | |
| NM_007299.3:c.787+194_787+195del | NP_009230.2:n.787+194_787+195del | |
| NM_007300.3:c.981_982del | NP_009231.2:p.Cys328Ter | |
| NR_027676.1:n.1117_1118del | ||
| NM_007294.4:c.981_982del MANE Select | NP_009225.1:p.Cys328Ter | |
| NM_007297.4:c.840_841del | NP_009228.2:p.Cys281Ter | |
| NM_007299.4:c.787+194_787+195del | NP_009230.2:n.787+194_787+195del | |
| NM_007300.4:c.981_982del | NP_009231.2:p.Cys328Ter | |
| NR_027676.2:n.1158_1159del |