Linked Data
gnomAD v4:
17-63945644-GGCCAGGGGGTCCATT-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63945650_63945664del , CM000679.2:g.63945650_63945664del | GRCh38 |
| NC_000017.10:g.62023010_62023024del , CM000679.1:g.62023010_62023024del | GRCh37 |
| NC_000017.9:g.59376742_59376756del | NCBI36 |
| NG_011699.1:g.32260_32274del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.3442-21_3442-7del MANE Select | ENSP00000396320.1:n.3442-21_3442-7del | |
| ENST00000578147.5:c.3442-21_3442-7del | ENSP00000463963.1:n.3442-21_3442-7del | |
| NM_000334.4:c.3442-21_3442-7del MANE Select | NP_000325.4:n.3442-21_3442-7del | |
| XM_005257566.3:c.3442-21_3442-7del | XP_005257623.1:n.3442-21_3442-7del |