HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169555193_169555194delinsTT , CM000663.2:g.169555193_169555194delinsTT | GRCh38 |
NC_000001.10:g.169524431_169524432delinsTT , CM000663.1:g.169524431_169524432delinsTT | GRCh37 |
NC_000001.9:g.167791055_167791056delinsTT | NCBI36 |
NG_011806.1:g.36338_36339delinsAA , LRG_553:g.36338_36339delinsAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.1106_1107delinsAA MANE Select | ENSP00000356771.3:p.Ala369Glu | |
ENST00000367796.3:c.1106_1107delinsAA | ENSP00000356770.3:p.Ala369Glu | |
ENST00000367797.7:c.1106_1107delinsAA | ENSP00000356771.3:p.Ala369Glu | |
NM_000130.4:c.1106_1107delinsAA , LRG_553t1:c.1106_1107delinsAA | NP_000121.2:p.Ala369Glu | |
XM_017000660.2:c.695_696delinsAA | XP_016856149.1:p.Ala232Glu | |
NM_000130.5:c.1106_1107delinsAA MANE Select | NP_000121.2:p.Ala369Glu |