Linked Data
gnomAD v4:
1-154571687-T-TA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571687_154571688insA , CM000663.2:g.154571687_154571688insA | GRCh38 |
| NC_000001.10:g.154544163_154544164insA , CM000663.1:g.154544163_154544164insA | GRCh37 |
| NC_000001.9:g.152810787_152810788insA | NCBI36 |
| NG_008027.1:g.8907_8908insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.864_865insA MANE Select | ENSP00000357461.3:p.Pro289ThrfsTer? | |
| ENST00000636034.1:c.864_865insA | ENSP00000489703.1:p.Pro289ThrfsTer? | |
| ENST00000637900.1:c.870_871insA | ENSP00000490474.1:p.Pro291ThrfsTer? | |
| ENST00000368476.3:c.864_865insA | ENSP00000357461.3:p.Pro289ThrfsTer? | |
| NM_000748.2:c.864_865insA | NP_000739.1:p.Pro289ThrfsTer? | |
| XM_017000180.2:c.354_355insA | XP_016855669.1:p.Pro119ThrfsTer? | |
| XR_001736952.2:n.1116_1117insA | ||
| NM_000748.3:c.864_865insA MANE Select | NP_000739.1:p.Pro289ThrfsTer? |