Linked Data
gnomAD v2:
15-89868894-CG-C
gnomAD v4:
15-89325663-CG-C
MyVariant Identifiers:
chr15:g.89868895del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89325668del , CM000677.2:g.89325668del | GRCh38 |
| NC_000015.9:g.89868899del , CM000677.1:g.89868899del | GRCh37 |
| NC_000015.8:g.87669903del | NCBI36 |
| NG_008218.1:g.14132del | |
| NG_008218.2:g.14132del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636937.2:c.1735del | ENSP00000516154.1:p.Arg579GlyfsTer2 | |
| ENST00000268124.11:c.1735del MANE Select | ENSP00000268124.5:p.Arg579GlyfsTer2 | |
| ENST00000530292.3:c.1336del | ENSP00000432885.2:p.Arg446GlyfsTer2 | |
| ENST00000635986.2:c.1735del | ENSP00000490653.2:p.Arg579GlyfsTer2 | |
| ENST00000636774.1:c.*302del | ENSP00000489799.1:n.*302del | |
| ENST00000637238.1:c.472del | ENSP00000490756.1:p.Arg158GlyfsTer2 | |
| ENST00000637264.1:c.807del | ||
| ENST00000666746.1:c.1312del | ||
| ENST00000670281.1:c.55del | ENSP00000499709.1:p.Arg19GlyfsTer2 | |
| ENST00000672071.1:n.1933del | ||
| ENST00000672923.2:n.1838del | ||
| ENST00000268124.9:c.1735del | ENSP00000268124.5:p.Arg579GlyfsTer2 | |
| ENST00000442287.6:c.1735del | ENSP00000399851.2:p.Arg579GlyfsTer2 | |
| ENST00000526314.2:c.117del | ||
| ENST00000631044.2:c.*1118del | ENSP00000486730.1:n.*1118del | |
| NM_001126131.1:c.1735del | NP_001119603.1:p.Arg579GlyfsTer2 | |
| NM_002693.2:c.1735del | NP_002684.1:p.Arg579GlyfsTer2 | |
| NM_001126131.2:c.1735del | NP_001119603.1:p.Arg579GlyfsTer2 | |
| NM_002693.3:c.1735del MANE Select | NP_002684.1:p.Arg579GlyfsTer2 |