HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215728445_215728446insC , CM000663.2:g.215728445_215728446insC | GRCh38 |
NC_000001.10:g.215901787_215901788insC , CM000663.1:g.215901787_215901788insC | GRCh37 |
NC_000001.9:g.213968410_213968411insC | NCBI36 |
NG_009497.1:g.699951_699952insG | |
NG_009497.2:g.700003_700004insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.11712-62_11712-61insG MANE Select | ENSP00000305941.3:n.11712-62_11712-61insG | |
ENST00000674083.1:c.11712-62_11712-61insG | ENSP00000501296.1:n.11712-62_11712-61insG | |
ENST00000307340.7:c.11712-62_11712-61insG | ENSP00000305941.3:n.11712-62_11712-61insG | |
NM_206933.2:c.11712-62_11712-61insG | NP_996816.2:n.11712-62_11712-61insG | |
NM_206933.3:c.11712-62_11712-61insG | NP_996816.2:n.11712-62_11712-61insG | |
NM_206933.4:c.11712-62_11712-61insG MANE Select | NP_996816.3:n.11712-62_11712-61insG |