Linked Data
gnomAD v4:
10-80273511-T-TC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80273511_80273512insC , CM000672.2:g.80273511_80273512insC | GRCh38 |
| NC_000010.10:g.82033267_82033268insC , CM000672.1:g.82033267_82033268insC | GRCh37 |
| NC_000010.9:g.82023247_82023248insC | NCBI36 |
| NG_008083.1:g.21167_21168insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.*269_*270insG MANE Select | ENSP00000361287.3:n.*269_*270insG | |
| ENST00000372213.7:c.*269_*270insG | ENSP00000361287.3:n.*269_*270insG | |
| ENST00000480845.1:n.620+69_620+70insG | ||
| ENST00000485270.5:n.969_970insG | ||
| NM_000429.2:c.*269_*270insG | NP_000420.1:n.*269_*270insG | |
| XM_005269842.3:c.*269_*270insG | XP_005269899.1:n.*269_*270insG | |
| XM_005269843.3:c.*269_*270insG | XP_005269900.1:n.*269_*270insG | |
| NM_000429.3:c.*269_*270insG MANE Select | NP_000420.1:n.*269_*270insG |