HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94782288_94782289insTG , CM000672.2:g.94782288_94782289insTG | GRCh38 |
NC_000010.10:g.96542045_96542046insTG , CM000672.1:g.96542045_96542046insTG | GRCh37 |
NC_000010.9:g.96532035_96532036insTG | NCBI36 |
NG_008384.2:g.24583_24584insTG | |
NG_008384.3:g.24608_24609insTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.819+291_819+292insTG MANE Select | ENSP00000360372.3:n.819+291_819+292insTG | |
ENST00000645461.1:n.1872+291_1872+292insTG | ||
ENST00000371321.7:c.819+291_819+292insTG | ENSP00000360372.3:n.819+291_819+292insTG | |
ENST00000464755.1:c.1582+291_1582+292insTG | ENSP00000483243.1:n.1582+291_1582+292insTG | |
NM_000769.2:c.819+291_819+292insTG | NP_000760.1:n.819+291_819+292insTG | |
NM_000769.4:c.819+291_819+292insTG MANE Select | NP_000760.1:n.819+291_819+292insTG |