HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10658463_10658465delinsCAT , CM000682.2:g.10658463_10658465delinsCAT | GRCh38 |
NC_000020.10:g.10639111_10639113delinsCAT , CM000682.1:g.10639111_10639113delinsCAT | GRCh37 |
NC_000020.9:g.10587111_10587113delinsCAT | NCBI36 |
NG_007496.1:g.20582_20584delinsATG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.694+3_694+5delinsATG MANE Select | ENSP00000254958.4:n.694+3_694+5delinsATG | |
ENST00000254958.9:c.694+3_694+5delinsATG | ENSP00000254958.4:n.694+3_694+5delinsATG | |
ENST00000423891.6:n.560+3_560+5delinsATG | ||
NM_000214.2:c.694+3_694+5delinsATG | NP_000205.1:n.694+3_694+5delinsATG | |
NM_000214.3:c.694+3_694+5delinsATG MANE Select | NP_000205.1:n.694+3_694+5delinsATG |