HGVS | Genome Assembly |
---|---|
NC_000002.12:g.84425593_84425594delinsGA , CM000664.2:g.84425593_84425594delinsGA | GRCh38 |
NC_000002.11:g.84652717_84652718delinsGA , CM000664.1:g.84652717_84652718delinsGA | GRCh37 |
NC_000002.10:g.84506228_84506229delinsGA | NCBI36 |
NG_016755.1:g.38869_38870delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393868.7:c.835_836delinsTC MANE Select | ENSP00000377446.2:p.Ser279= | |
ENST00000651342.1:c.*275_*276delinsTC | ENSP00000498471.1:n.*275_*276delinsTC | |
ENST00000393868.6:c.835_836delinsTC | ENSP00000377446.2:p.Ser279= | |
ENST00000484365.1:n.1343_1344delinsTC | ||
ENST00000487809.1:n.582_583delinsTC | ||
ENST00000491123.5:n.681_682delinsTC | ||
NM_003849.3:c.835_836delinsTC | NP_003840.2:p.Ser279= | |
NM_003849.4:c.835_836delinsTC MANE Select | NP_003840.2:p.Ser279= |