HGVS | Genome Assembly |
---|---|
NC_000003.12:g.138945868_138945885del , CM000665.2:g.138945868_138945885del | GRCh38 |
NC_000003.11:g.138664710_138664727del , CM000665.1:g.138664710_138664727del | GRCh37 |
NC_000003.10:g.140147400_140147417del | NCBI36 |
NG_012454.1:g.6258_6275del | |
NG_029796.1:g.3635_3652del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648323.1:c.840_857del MANE Select | ENSP00000497217.1:p.Pro281_Pro286del | |
ENST00000330315.3:c.840_857del | ENSP00000333188.3:p.Pro281_Pro286del | |
NM_023067.3:c.840_857del | NP_075555.1:p.Pro281_Pro286del | |
NM_023067.4:c.840_857del MANE Select | NP_075555.1:p.Pro281_Pro286del |