Linked Data
gnomAD v4:
21-34370539-A-ACAACTT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34370540_34370541insAACTTC , CM000683.2:g.34370540_34370541insAACTTC | GRCh38 |
| NC_000021.8:g.35742839_35742840insAACTTC , CM000683.1:g.35742839_35742840insAACTTC | GRCh37 |
| NC_000021.7:g.34664709_34664710insAACTTC | NCBI36 |
| NG_008804.1:g.11517_11518insAACTTC , LRG_291:g.11517_11518insAACTTC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290310.4:c.62_63insAACTTC MANE Select | ENSP00000290310.2:p.Thr21_Tyr22insThrSer | |
| ENST00000290310.3:c.62_63insAACTTC | ENSP00000290310.2:p.Thr21_Tyr22insThrSer | |
| NM_172201.1:c.62_63insAACTTC , LRG_291t1:c.62_63insAACTTC | NP_751951.1:p.Thr21_Tyr22insThrSer | |
| XR_937683.1:n.781_782insAAGTTG | ||
| XR_937684.1:n.781_782insAAGTTG | ||
| XR_001755012.2:n.902_903insAAGTTG | ||
| XR_001755013.2:n.781_782insAAGTTG | ||
| XR_937683.2:n.781_782insAAGTTG | ||
| NM_172201.2:c.62_63insAACTTC MANE Select | NP_751951.1:p.Thr21_Tyr22insThrSer |