Linked Data
gnomAD v4:
10-122461604-T-TTCTC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122461604_122461605insTCTC , CM000672.2:g.122461604_122461605insTCTC | GRCh38 |
| NC_000010.10:g.124221120_124221121insTCTC , CM000672.1:g.124221120_124221121insTCTC | GRCh37 |
| NC_000010.9:g.124211110_124211111insTCTC | NCBI36 |
| NG_011554.1:g.5080_5081insTCTC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.-49_-48insTCTC MANE Select | ENSP00000357980.3:n.-49_-48insTCTC | |
| ENST00000648167.1:c.154+2895_154+2896insTCTC | ENSP00000498033.1:n.154+2895_154+2896insTCTC | |
| ENST00000368984.7:c.-49_-48insTCTC | ENSP00000357980.3:n.-49_-48insTCTC | |
| NM_002775.4:c.-49_-48insTCTC | NP_002766.1:n.-49_-48insTCTC | |
| NM_002775.5:c.-49_-48insTCTC MANE Select | NP_002766.1:n.-49_-48insTCTC |