Linked Data
gnomAD v4:
7-129213177-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.129213177_129213178insA , CM000669.2:g.129213177_129213178insA | GRCh38 |
| NC_000007.13:g.128853018_128853019insA , CM000669.1:g.128853018_128853019insA | GRCh37 |
| NC_000007.12:g.128640254_128640255insA | NCBI36 |
| NG_023340.1:g.29306_29307insA | |
| NG_023340.2:g.29306_29307insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249373.8:c.*726_*727insA MANE Select | ENSP00000249373.3:n.*726_*727insA | |
| ENST00000655644.1:c.*2845_*2846insA | ENSP00000499377.1:n.*2845_*2846insA | |
| ENST00000249373.7:c.*726_*727insA | ENSP00000249373.3:n.*726_*727insA | |
| NM_005631.4:c.*726_*727insA | NP_005622.1:n.*726_*727insA | |
| XM_011516522.1:c.*726_*727insA | XP_011514824.1:n.*726_*727insA | |
| XM_024446891.1:c.*726_*727insA | XP_024302659.1:n.*726_*727insA | |
| NM_005631.5:c.*726_*727insA MANE Select | NP_005622.1:n.*726_*727insA |