Linked Data
gnomAD v4:
6-121447513-C-CTT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.121447514_121447515dup , CM000668.2:g.121447514_121447515dup | GRCh38 |
| NC_000006.11:g.121768660_121768661dup , CM000668.1:g.121768660_121768661dup | GRCh37 |
| NC_000006.10:g.121810359_121810360dup | NCBI36 |
| NG_008308.1:g.16916_16917dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282561.4:c.667_668dup MANE Select | ENSP00000282561.3:p.Leu223PhefsTer2 | |
| ENST00000647564.1:c.667_668dup | ENSP00000497565.1:p.Leu223PhefsTer2 | |
| ENST00000649003.1:c.667_668dup | ENSP00000497283.1:p.Leu223PhefsTer2 | |
| ENST00000650427.1:c.667_668dup | ENSP00000497367.1:p.Leu223PhefsTer2 | |
| ENST00000282561.3:c.667_668dup | ENSP00000282561.3:p.Leu223PhefsTer2 | |
| NM_000165.4:c.667_668dup | NP_000156.1:p.Leu223PhefsTer2 | |
| NM_000165.5:c.667_668dup MANE Select | NP_000156.1:p.Leu223PhefsTer2 |