HGVS | Genome Assembly |
---|---|
NC_000009.12:g.114785425_114785427del , CM000671.2:g.114785425_114785427del | GRCh38 |
NC_000009.11:g.117547705_117547707del , CM000671.1:g.117547705_117547707del | GRCh37 |
NC_000009.10:g.116587526_116587528del | NCBI36 |
NG_011488.2:g.25704_25706del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374045.5:c.*5027_*5029del MANE Select | ENSP00000363157.3:n.*5027_*5029del | |
ENST00000374045.4:c.*5027_*5029del | ENSP00000363157.3:n.*5027_*5029del | |
NM_001204344.1:c.5606_5608del | NP_001191273.1:n.5606_5608del | |
NM_005118.3:c.*5027_*5029del | NP_005109.2:n.*5027_*5029del | |
NM_005118.4:c.*5027_*5029del MANE Select | NP_005109.2:n.*5027_*5029del |