HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32220454_32220499del , CM000668.2:g.32220454_32220499del | GRCh38 |
NC_000006.11:g.32188231_32188276del , CM000668.1:g.32188231_32188276del | GRCh37 |
NC_000006.10:g.32296209_32296254del | NCBI36 |
NG_028190.1:g.8569_8614del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.1065_1110del MANE Select | ENSP00000364163.3:p.Asn355LysfsTer28 | |
ENST00000473562.1:n.1194_1239del | ||
NM_004557.3:c.1065_1110del | NP_004548.3:p.Asn355LysfsTer28 | |
NR_134949.1:n.1204_1249del | ||
NR_134950.1:n.1204_1249del | ||
NM_004557.4:c.1065_1110del MANE Select | NP_004548.3:p.Asn355LysfsTer28 | |
NR_134949.2:n.1204_1249del | ||
NR_134950.2:n.1204_1249del |