HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20189482_20189483delinsTA , CM000675.2:g.20189482_20189483delinsTA | GRCh38 |
NC_000013.10:g.20763621_20763622delinsTA , CM000675.1:g.20763621_20763622delinsTA | GRCh37 |
NC_000013.9:g.19661621_19661622delinsTA | NCBI36 |
NG_008358.1:g.8493_8494delinsTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.99_100delinsTA | ENSP00000372295.1:p.Ile33= | |
ENST00000382848.5:c.99_100delinsTA MANE Select | ENSP00000372299.4:p.Ile33= | |
ENST00000382844.1:c.99_100delinsTA | ENSP00000372295.1:p.Ile33= | |
ENST00000382848.4:c.99_100delinsTA | ENSP00000372299.4:p.Ile33= | |
NM_004004.5:c.99_100delinsTA | NP_003995.2:p.Ile33= | |
XM_011535049.1:c.99_100delinsTA | XP_011533351.1:p.Ile33= | |
XM_011535049.2:c.99_100delinsTA | XP_011533351.1:p.Ile33= | |
NM_004004.6:c.99_100delinsTA MANE Select | NP_003995.2:p.Ile33= |