Linked Data
gnomAD v4:
21-44287257-T-TG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44287262dup , CM000683.2:g.44287262dup | GRCh38 |
| NC_000021.8:g.45707145dup , CM000683.1:g.45707145dup | GRCh37 |
| NC_000021.7:g.44531573dup | NCBI36 |
| NG_009556.1:g.6383dup , LRG_18:g.6383dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.463+129dup MANE Select | ENSP00000291582.5:n.463+129dup | |
| ENST00000291582.5:c.463+129dup | ENSP00000291582.5:n.463+129dup | |
| ENST00000527919.5:n.753dup | ||
| ENST00000530812.5:n.761dup | ||
| NM_000383.3:c.463+129dup | NP_000374.1:n.463+129dup | |
| XM_011529551.1:c.463+129dup | XP_011527853.1:n.463+129dup | |
| NM_000383.4:c.463+129dup MANE Select | NP_000374.1:n.463+129dup |