HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10650238_10650239delinsTG , CM000682.2:g.10650238_10650239delinsTG | GRCh38 |
NC_000020.10:g.10630886_10630887delinsTG , CM000682.1:g.10630886_10630887delinsTG | GRCh37 |
NC_000020.9:g.10578886_10578887delinsTG | NCBI36 |
NG_007496.1:g.28808_28809delinsCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000254958.10:c.1234+8_1234+9delinsCA MANE Select | ENSP00000254958.4:n.1234+8_1234+9delinsCA... | |
ENST00000617965.2:n.1823+8_1823+9delinsCA | ||
ENST00000254958.9:c.1234+8_1234+9delinsCA | ENSP00000254958.4:n.1234+8_1234+9delinsCA... | |
ENST00000423891.6:n.1100+8_1100+9delinsCA | ||
ENST00000622545.1:c.11+8_11+9delinsCA | ||
NM_000214.2:c.1234+8_1234+9delinsCA | NP_000205.1:n.1234+8_1234+9delinsCA | |
NM_000214.3:c.1234+8_1234+9delinsCA MANE Select | NP_000205.1:n.1234+8_1234+9delinsCA |