Linked Data
gnomAD v4:
22-27750642-A-AGCT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.27750643_27750644insCTG , CM000684.2:g.27750643_27750644insCTG | GRCh38 |
| NC_000022.10:g.28146631_28146632insCTG , CM000684.1:g.28146631_28146632insCTG | GRCh37 |
| NC_000022.9:g.26476631_26476632insCTG | NCBI36 |
| NG_023258.1:g.55856_55857insAGC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703102.1:n.760_761insAGC | ||
| ENST00000302326.5:c.*272_*273insAGC MANE Select | ENSP00000304956.4:n.*272_*273insAGC | |
| ENST00000302326.4:c.*272_*273insAGC | ENSP00000304956.4:n.*272_*273insAGC | |
| ENST00000424656.1:c.455+133_455+134insAGC | ||
| NM_002430.2:c.*272_*273insAGC | NP_002421.3:n.*272_*273insAGC | |
| NM_002430.3:c.*272_*273insAGC MANE Select | NP_002421.3:n.*272_*273insAGC |