Linked Data
gnomAD v2:
17-17697094-CA-C
gnomAD v4:
17-17793780-CA-C
MyVariant Identifiers:
chr17:g.17697095del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.17793781del , CM000679.2:g.17793781del | GRCh38 |
| NC_000017.10:g.17697095del , CM000679.1:g.17697095del | GRCh37 |
| NC_000017.9:g.17637820del | NCBI36 |
| NG_007101.2:g.117309del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000353383.6:c.833del MANE Select | ENSP00000323074.4:p.Gln278ArgfsTer? | |
| ENST00000640861.1:c.767del | ENSP00000491773.1:p.Gln256ArgfsTer? | |
| ENST00000353383.5:c.833del | ENSP00000323074.4:p.Gln278ArgfsTer? | |
| ENST00000395774.1:c.833del | ENSP00000379120.1:p.Gln278ArgfsTer? | |
| NM_030665.3:c.833del | NP_109590.3:p.Gln278ArgfsTer? | |
| XM_017024025.1:c.833del | XP_016879514.1:p.Gln278ArgfsTer? | |
| XM_017024026.1:c.833del | XP_016879515.1:p.Gln278ArgfsTer? | |
| XM_017024027.1:c.833del | XP_016879516.1:p.Gln278ArgfsTer? | |
| XM_017024028.2:c.833del | XP_016879517.1:p.Gln278ArgfsTer? | |
| NM_030665.4:c.833del MANE Select | NP_109590.3:p.Gln278ArgfsTer? |