ClinVar RCV:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43094733_43094734del , CM000679.2:g.43094733_43094734del | GRCh38 |
| NC_000017.10:g.41246750_41246751del , CM000679.1:g.41246750_41246751del | GRCh37 |
| NC_000017.9:g.38500276_38500277del | NCBI36 |
| NG_005905.2:g.123251_123252del , LRG_292:g.123251_123252del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.862_863del | ||
| ENST00000461574.2:c.798_799del | ENSP00000417241.2:p.Ser267LysfsTer19 | |
| ENST00000470026.6:c.798_799del | ENSP00000419274.2:p.Ser267LysfsTer19 | |
| ENST00000473961.6:c.672_673del | ENSP00000420201.2:p.Ser225LysfsTer19 | |
| ENST00000476777.6:c.795_796del | ENSP00000417554.2:p.Ser266LysfsTer19 | |
| ENST00000477152.6:c.720_721del | ENSP00000419988.2:p.Ser241LysfsTer19 | |
| ENST00000478531.6:c.784+11_784+12del | ENSP00000420412.2:n.784+11_784+12del | |
| ENST00000489037.2:c.720_721del | ENSP00000420781.2:p.Ser241LysfsTer19 | |
| ENST00000493919.6:c.646+11_646+12del | ENSP00000418819.2:n.646+11_646+12del | |
| ENST00000494123.6:c.798_799del | ENSP00000419103.2:p.Ser267LysfsTer19 | |
| ENST00000497488.2:c.-91_-90del | ENSP00000418986.2:n.-91_-90del | |
| ENST00000618469.2:c.798_799del | ENSP00000478114.2:p.Ser267LysfsTer19 | |
| ENST00000634433.2:c.675_676del | ENSP00000489431.2:p.Ser226LysfsTer19 | |
| ENST00000644379.2:c.798_799del | ENSP00000496570.2:p.Ser267LysfsTer19 | |
| ENST00000644555.2:c.646+11_646+12del | ENSP00000494614.2:n.646+11_646+12del | |
| ENST00000652672.2:c.657_658del | ENSP00000498906.2:p.Ser220LysfsTer19 | |
| ENST00000484087.6:c.664+11_664+12del | ENSP00000419481.2:n.664+11_664+12del | |
| ENST00000700182.1:c.706+11_706+12del | ENSP00000514849.1:n.706+11_706+12del | |
| ENST00000700183.1:c.*806_*807del | ENSP00000514850.1:n.*806_*807del | |
| ENST00000357654.9:c.798_799del MANE Select | ENSP00000350283.3:p.Ser267LysfsTer19 | |
| ENST00000471181.7:c.798_799del | ENSP00000418960.2:p.Ser267LysfsTer19 | |
| ENST00000642945.1:c.*672_*673del | ENSP00000495897.1:n.*672_*673del | |
| ENST00000652672.1:c.657_658del | ENSP00000498906.1:p.Ser220LysfsTer19 | |
| ENST00000352993.7:c.670+1113_670+1114del | ENSP00000312236.5:n.670+1113_670+1114del | |
| ENST00000354071.7:c.798_799del | ENSP00000326002.7:p.Ser267LysfsTer19 | |
| ENST00000357654.7:c.798_799del | ENSP00000350283.3:p.Ser267LysfsTer19 | |
| ENST00000412061.3:c.149_150del | ||
| ENST00000461221.5:c.*581_*582del | ENSP00000418548.1:n.*581_*582del | |
| ENST00000468300.5:c.787+11_787+12del | ENSP00000417148.1:n.787+11_787+12del | |
| ENST00000470026.5:c.798_799del | ENSP00000419274.1:p.Ser267LysfsTer19 | |
| ENST00000471181.6:c.798_799del | ENSP00000418960.2:p.Ser267LysfsTer19 | |
| ENST00000473961.5:c.395_396del | ||
| ENST00000477152.5:c.720_721del | ENSP00000419988.1:p.Ser241LysfsTer19 | |
| ENST00000478531.5:c.784+11_784+12del | ENSP00000420412.1:n.784+11_784+12del | |
| ENST00000484087.5:c.409+11_409+12del | ENSP00000419481.1:n.409+11_409+12del | |
| ENST00000487825.5:c.412+11_412+12del | ENSP00000418212.1:n.412+11_412+12del | |
| ENST00000491747.6:c.787+11_787+12del | ENSP00000420705.2:n.787+11_787+12del | |
| ENST00000492859.5:c.*734_*735del | ENSP00000420253.1:n.*734_*735del | |
| ENST00000493795.5:c.657_658del | ENSP00000418775.1:p.Ser220LysfsTer19 | |
| ENST00000493919.5:c.646+11_646+12del | ENSP00000418819.1:n.646+11_646+12del | |
| ENST00000494123.5:c.798_799del | ENSP00000419103.1:p.Ser267LysfsTer19 | |
| ENST00000497488.1:c.-91_-90del | ENSP00000418986.1:n.-91_-90del | |
| ENST00000586385.5:c.4+30449_4+30450del | ENSP00000465818.1:n.4+30449_4+30450del | |
| ENST00000591534.5:c.-43-20212_-43-20211del | ENSP00000467329.1:n.-43-20212_-43-20211del | |
| ENST00000591849.5:c.-99+30538_-99+30539del | ENSP00000465347.1:n.-99+30538_-99+30539del | |
| ENST00000634433.1:c.675_676del | ENSP00000489431.1:p.Ser226LysfsTer19 | |
| NM_007294.3:c.798_799del , LRG_292t1:c.798_799del | NP_009225.1:p.Ser267LysfsTer19 | |
| NM_007297.3:c.657_658del | NP_009228.2:p.Ser220LysfsTer19 | |
| NM_007298.3:c.787+11_787+12del | NP_009229.2:n.787+11_787+12del | |
| NM_007299.3:c.787+11_787+12del | NP_009230.2:n.787+11_787+12del | |
| NM_007300.3:c.798_799del | NP_009231.2:p.Ser267LysfsTer19 | |
| NR_027676.1:n.934_935del | ||
| NM_007294.4:c.798_799del MANE Select | NP_009225.1:p.Ser267LysfsTer19 | |
| NM_007297.4:c.657_658del | NP_009228.2:p.Ser220LysfsTer19 | |
| NM_007299.4:c.787+11_787+12del | NP_009230.2:n.787+11_787+12del | |
| NM_007300.4:c.798_799del | NP_009231.2:p.Ser267LysfsTer19 | |
| NR_027676.2:n.975_976del |