Linked Data
gnomAD v4:
17-63941754-CCTT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63941758_63941760del , CM000679.2:g.63941758_63941760del | GRCh38 |
| NC_000017.10:g.62019118_62019120del , CM000679.1:g.62019118_62019120del | GRCh37 |
| NC_000017.9:g.59372850_59372852del | NCBI36 |
| NG_011699.1:g.36162_36164del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.4525_4527del MANE Select | ENSP00000396320.1:p.Lys1509del | |
| ENST00000578147.5:c.4525_4527del | ENSP00000463963.1:p.Lys1509del | |
| NM_000334.4:c.4525_4527del MANE Select | NP_000325.4:p.Lys1509del | |
| XM_005257566.3:c.4525_4527del | XP_005257623.1:p.Lys1509del |