HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215817248_215817249insACA , CM000663.2:g.215817248_215817249insACA | GRCh38 |
NC_000001.10:g.215990590_215990591insACA , CM000663.1:g.215990590_215990591insACA | GRCh37 |
NC_000001.9:g.214057213_214057214insACA | NCBI36 |
NG_009497.1:g.611148_611149insTGT | |
NG_009497.2:g.611200_611201insTGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.9372-54_9372-53insTGT MANE Select | ENSP00000305941.3:n.9372-54_9372-53insTGT | |
ENST00000674083.1:c.9372-54_9372-53insTGT | ENSP00000501296.1:n.9372-54_9372-53insTGT | |
ENST00000307340.7:c.9372-54_9372-53insTGT | ENSP00000305941.3:n.9372-54_9372-53insTGT | |
NM_206933.2:c.9372-54_9372-53insTGT | NP_996816.2:n.9372-54_9372-53insTGT | |
NM_206933.3:c.9372-54_9372-53insTGT | NP_996816.2:n.9372-54_9372-53insTGT | |
NM_206933.4:c.9372-54_9372-53insTGT MANE Select | NP_996816.3:n.9372-54_9372-53insTGT |