HGVS | Genome Assembly |
---|---|
NC_000023.11:g.64192013_64192015del , CM000685.2:g.64192013_64192015del | GRCh38 |
NC_000023.10:g.63411893_63411895del , CM000685.1:g.63411893_63411895del | GRCh37 |
NC_000023.9:g.63328618_63328620del | NCBI36 |
NG_021345.1:g.18731_18733del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374869.8:c.1273_1275del MANE Select | ENSP00000364003.4:p.Tyr425del | |
ENST00000330258.3:c.1273_1275del | ENSP00000329117.3:p.Tyr425del | |
ENST00000374869.7:c.1273_1275del | ENSP00000364003.3:p.Tyr425del | |
NM_152424.3:c.1273_1275del | NP_689637.3:p.Tyr425del | |
XM_011530858.1:c.1273_1275del | XP_011529160.1:p.Tyr425del | |
NM_152424.4:c.1273_1275del MANE Select | NP_689637.3:p.Tyr425del |