HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1394882_1394883delinsTG , CM000667.2:g.1394882_1394883delinsTG | GRCh38 |
NC_000005.9:g.1394997_1394998delinsTG , CM000667.1:g.1394997_1394998delinsTG | GRCh37 |
NC_000005.8:g.1447997_1447998delinsTG | NCBI36 |
NG_015885.1:g.55546_55547delinsCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000270349.12:c.1840-125_1840-124delinsCA MANE Select | ENSP00000270349.9:n.1840-125_1840-124deli... | |
ENST00000270349.11:c.1840-125_1840-124delinsCA | ENSP00000270349.9:n.1840-125_1840-124deli... | |
ENST00000512002.2:n.221-125_221-124delinsCA | ||
NM_001044.4:c.1840-125_1840-124delinsCA | NP_001035.1:n.1840-125_1840-124delinsCA | |
NM_001044.5:c.1840-125_1840-124delinsCA MANE Select | NP_001035.1:n.1840-125_1840-124delinsCA |