HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215728438_215728448del , CM000663.2:g.215728438_215728448del | GRCh38 |
NC_000001.10:g.215901780_215901790del , CM000663.1:g.215901780_215901790del | GRCh37 |
NC_000001.9:g.213968403_213968413del | NCBI36 |
NG_009497.1:g.699950_699960del | |
NG_009497.2:g.700002_700012del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.11712-63_11712-53del MANE Select | ENSP00000305941.3:n.11712-63_11712-53del | |
ENST00000674083.1:c.11712-63_11712-53del | ENSP00000501296.1:n.11712-63_11712-53del | |
ENST00000307340.7:c.11712-63_11712-53del | ENSP00000305941.3:n.11712-63_11712-53del | |
NM_206933.2:c.11712-63_11712-53del | NP_996816.2:n.11712-63_11712-53del | |
NM_206933.3:c.11712-63_11712-53del | NP_996816.2:n.11712-63_11712-53del | |
NM_206933.4:c.11712-63_11712-53del MANE Select | NP_996816.3:n.11712-63_11712-53del |