Linked Data
gnomAD v2:
17-27861127-CTG-C
gnomAD v4:
17-29534109-CTG-C
MyVariant Identifiers:
chr17:g.27861128_27861129del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29534111_29534112del , CM000679.2:g.29534111_29534112del | GRCh38 |
| NC_000017.10:g.27861129_27861130del , CM000679.1:g.27861129_27861130del | GRCh37 |
| NC_000017.9:g.24885255_24885256del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261716.8:c.2362-7_2362-6del MANE Select | ENSP00000261716.3:n.2362-7_2362-6del | |
| ENST00000261716.7:c.2362-7_2362-6del | ENSP00000261716.3:n.2362-7_2362-6del | |
| ENST00000536202.1:c.1918-7_1918-6del | ENSP00000438819.1:n.1918-7_1918-6del | |
| NM_020791.2:c.2362-7_2362-6del | NP_065842.1:n.2362-7_2362-6del | |
| NM_025142.1:c.1918-7_1918-6del | NP_079418.1:n.1918-7_1918-6del | |
| XM_011525060.1:c.2362-7_2362-6del | XP_011523362.1:n.2362-7_2362-6del | |
| XM_011525060.2:c.2362-7_2362-6del | XP_011523362.1:n.2362-7_2362-6del | |
| NM_020791.4:c.2362-7_2362-6del MANE Select | NP_065842.1:n.2362-7_2362-6del |