Linked Data
gnomAD v4:
16-81358012-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81358016del , CM000678.2:g.81358016del | GRCh38 |
| NC_000016.9:g.81391621del , CM000678.1:g.81391621del | GRCh37 |
| NC_000016.8:g.79949122del | NCBI36 |
| NG_009007.1:g.48051del , LRG_242:g.48051del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648349.2:c.*681+85del | ENSP00000498114.1:n.*681+85del | |
| ENST00000648994.2:c.973+85del MANE Select | ENSP00000497351.1:n.973+85del | |
| ENST00000650388.1:c.507+85del | ENSP00000498081.1:n.507+85del | |
| ENST00000568107.2:c.973+85del | ENSP00000476795.1:n.973+85del | |
| NM_022041.3:c.973+85del , LRG_242t1:c.973+85del | NP_071324.1:n.973+85del | |
| XM_017023734.1:c.334+85del | XP_016879223.1:n.334+85del | |
| NM_001377486.1:c.334+85del | NP_001364415.1:n.334+85del | |
| NM_022041.4:c.973+85del MANE Select | NP_071324.1:n.973+85del |