HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21174565_21174575delinsTTCCCTTTCTA , CM000674.2:g.21174565_21174575delinsTTCCCTTTCTA | GRCh38 |
NC_000012.11:g.21327499_21327509delinsTTCCCTTTCTA , CM000674.1:g.21327499_21327509delinsTTCCCTTTCTA | GRCh37 |
NC_000012.10:g.21218766_21218776delinsTTCCCTTTCTA | NCBI36 |
NG_011745.1:g.48372_48382delinsTTCCCTTTCTA , LRG_1022:g.48372_48382delinsTTCCCTTTCTA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.227-12_227-2delinsTTCCCTTTCTA MANE Select | ENSP00000256958.2:n.227-12_227-2delinsTTC... | |
ENST00000256958.2:c.227-12_227-2delinsTTCCCTTTCTA | ENSP00000256958.2:n.227-12_227-2delinsTTC... | |
ENST00000543498.5:c.426-2211_426-2201delinsTTCCCTTTCTA | ||
NM_006446.4:c.227-12_227-2delinsTTCCCTTTCTA , LRG_1022t1:c.227-12_227-2delinsTTCCCTTTCTA | NP_006437.3:n.227-12_227-2delinsTTCCCTTTC... | |
NM_006446.5:c.227-12_227-2delinsTTCCCTTTCTA MANE Select | NP_006437.3:n.227-12_227-2delinsTTCCCTTTC... |