HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713655_6713656insTC , CM000681.2:g.6713655_6713656insTC | GRCh38 |
NC_000019.9:g.6713666_6713667insTC , CM000681.1:g.6713666_6713667insTC | GRCh37 |
NC_000019.8:g.6664666_6664667insTC | NCBI36 |
NG_009557.1:g.11997_11998insAG , LRG_27:g.11997_11998insAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.651-146_651-145insAG | ENSP00000512083.1:n.651-146_651-145insAG | |
ENST00000245907.11:c.774-146_774-145insAG MANE Select | ENSP00000245907.4:n.774-146_774-145insAG | |
ENST00000245907.10:c.774-146_774-145insAG | ENSP00000245907.4:n.774-146_774-145insAG | |
ENST00000595577.1:n.278-146_278-145insAG | ||
ENST00000597442.5:n.23+111_23+112insAG | ||
NM_000064.3:c.774-146_774-145insAG | NP_000055.2:n.774-146_774-145insAG | |
NM_000064.4:c.774-146_774-145insAG MANE Select | NP_000055.2:n.774-146_774-145insAG |