Linked Data
gnomAD v4:
1-154571699-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571699_154571700insA , CM000663.2:g.154571699_154571700insA | GRCh38 |
| NC_000001.10:g.154544175_154544176insA , CM000663.1:g.154544175_154544176insA | GRCh37 |
| NC_000001.9:g.152810799_152810800insA | NCBI36 |
| NG_008027.1:g.8919_8920insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.876_877insA MANE Select | ENSP00000357461.3:p.Asp293ArgfsTer? | |
| ENST00000636034.1:c.876_877insA | ENSP00000489703.1:p.Asp293ArgfsTer? | |
| ENST00000637900.1:c.882_883insA | ENSP00000490474.1:p.Asp295ArgfsTer? | |
| ENST00000368476.3:c.876_877insA | ENSP00000357461.3:p.Asp293ArgfsTer? | |
| NM_000748.2:c.876_877insA | NP_000739.1:p.Asp293ArgfsTer? | |
| XM_017000180.2:c.366_367insA | XP_016855669.1:p.Asp123ArgfsTer? | |
| XR_001736952.2:n.1128_1129insA | ||
| NM_000748.3:c.876_877insA MANE Select | NP_000739.1:p.Asp293ArgfsTer? |