HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47004099_47004100delinsCG , CM000681.2:g.47004099_47004100delinsCG | GRCh38 |
NC_000019.9:g.47507356_47507357delinsCG , CM000681.1:g.47507356_47507357delinsCG | GRCh37 |
NC_000019.8:g.52199196_52199197delinsCG | NCBI36 |
NG_047014.1:g.90533_90534delinsCG | |
NG_047014.2:g.148103_148104delinsCG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000404338.8:c.7911_7912delinsCG | ENSP00000385720.2:n.7911_7912delinsCG | |
ENST00000672722.1:c.*3411_*3412delinsCG MANE Select | ENSP00000500409.1:n.*3411_*3412delinsCG | |
ENST00000404338.7:c.7911_7912delinsCG | ENSP00000385720.2:n.7911_7912delinsCG | |
ENST00000614079.1:c.7488_7489delinsCG | ENSP00000483730.1:n.7488_7489delinsCG | |
NM_004491.4:c.7911_7912delinsCG | NP_004482.4:n.7911_7912delinsCG | |
NM_004491.5:c.*3411_*3412delinsCG MANE Select | NP_004482.4:n.*3411_*3412delinsCG |