HGVS | Genome Assembly |
---|---|
NC_000011.10:g.64759930_64759931insTAG , CM000673.2:g.64759930_64759931insTAG | GRCh38 |
NC_000011.9:g.64527402_64527403insTAG , CM000673.1:g.64527402_64527403insTAG | GRCh37 |
NC_000011.8:g.64283978_64283979insTAG | NCBI36 |
NG_013018.1:g.5785_5786insCTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000164139.4:c.-33_-32insCTA MANE Select | ENSP00000164139.3:n.-33_-32insCTA | |
ENST00000164139.3:c.-33_-32insCTA | ENSP00000164139.3:n.-33_-32insCTA | |
ENST00000377432.7:c.-33_-32insCTA | ENSP00000366650.3:n.-33_-32insCTA | |
NM_001164716.1:c.-33_-32insCTA | NP_001158188.1:n.-33_-32insCTA | |
NM_005609.2:c.-33_-32insCTA | NP_005600.1:n.-33_-32insCTA | |
NM_005609.3:c.-33_-32insCTA | NP_005600.1:n.-33_-32insCTA | |
NM_005609.4:c.-33_-32insCTA MANE Select | NP_005600.1:n.-33_-32insCTA |