Linked Data
gnomAD v4:
X-8731821-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.8731825del , CM000685.2:g.8731825del | GRCh38 |
| NC_000023.10:g.8699866del , CM000685.1:g.8699866del | GRCh37 |
| NC_000023.9:g.8659866del | NCBI36 |
| NG_007088.1:g.5365del | |
| NG_007088.2:g.5365del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262648.8:c.207+8del MANE Select | ENSP00000262648.3:n.207+8del | |
| ENST00000262648.7:c.207+8del | ENSP00000262648.3:n.207+8del | |
| ENST00000619786.1:c.204+8del | ENSP00000478734.1:n.204+8del | |
| NM_000216.2:c.207+8del | NP_000207.2:n.207+8del | |
| XM_005274501.3:c.207+8del | XP_005274558.1:n.207+8del | |
| NM_000216.3:c.207+8del | NP_000207.2:n.207+8del | |
| XM_005274501.4:c.207+8del | XP_005274558.1:n.207+8del | |
| NM_000216.4:c.207+8del MANE Select | NP_000207.2:n.207+8del |