Linked Data
gnomAD v4:
X-154379396-GC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154379401del , CM000685.2:g.154379401del | GRCh38 |
| NC_000023.10:g.153607761del , CM000685.1:g.153607761del | GRCh37 |
| NC_000023.9:g.153260955del | NCBI36 |
| NG_008677.1:g.9966del , LRG_745:g.9966del | |
| NG_011506.1:g.250del | |
| NG_011506.2:g.242del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369842.9:c.-84del MANE Select | ENSP00000358857.4:n.-84del | |
| ENST00000369835.3:c.-84del | ENSP00000358850.3:n.-84del | |
| ENST00000369842.8:c.-84del | ENSP00000358857.4:n.-84del | |
| ENST00000428228.5:c.-84del | ENSP00000401081.1:n.-84del | |
| ENST00000486738.5:n.61del | ||
| NM_000117.2:c.-84del , LRG_745t1:c.-84del | NP_000108.1:n.-84del | |
| XM_024452349.1:c.-292del | XP_024308117.1:n.-292del | |
| NM_000117.3:c.-84del MANE Select | NP_000108.1:n.-84del |