HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47003877_47003878insA , CM000681.2:g.47003877_47003878insA | GRCh38 |
NC_000019.9:g.47507134_47507135insA , CM000681.1:g.47507134_47507135insA | GRCh37 |
NC_000019.8:g.52198974_52198975insA | NCBI36 |
NG_047014.1:g.90311_90312insA | |
NG_047014.2:g.147881_147882insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.7689_7690insA | ENSP00000385720.2:n.7689_7690insA | |
ENST00000672722.1:c.*3189_*3190insA MANE Select | ENSP00000500409.1:n.*3189_*3190insA | |
ENST00000404338.7:c.7689_7690insA | ENSP00000385720.2:n.7689_7690insA | |
ENST00000614079.1:c.7266_7267insA | ENSP00000483730.1:n.7266_7267insA | |
NM_004491.4:c.7689_7690insA | NP_004482.4:n.7689_7690insA | |
NM_004491.5:c.*3189_*3190insA MANE Select | NP_004482.4:n.*3189_*3190insA |