HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99949751_99949753del , CM000666.2:g.99949751_99949753del | GRCh38 |
NC_000004.11:g.100870908_100870910del , CM000666.1:g.100870908_100870910del | GRCh37 |
NC_000004.10:g.101089931_101089933del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296417.6:c.4-13_4-11del MANE Select | ENSP00000296417.5:n.4-13_4-11del | |
ENST00000651623.1:c.4-13_4-11del | ENSP00000498935.1:n.4-13_4-11del | |
ENST00000296417.5:c.4-13_4-11del | ENSP00000296417.5:n.4-13_4-11del | |
ENST00000511203.1:n.547_549del | ||
ENST00000511319.5:n.516_518del | ||
ENST00000511348.1:n.189-13_189-11del | ||
ENST00000527366.1:n.88-13_88-11del | ||
ENST00000529158.5:n.53-13_53-11del | ||
NM_002106.3:c.4-13_4-11del | NP_002097.1:n.4-13_4-11del | |
NM_002106.4:c.4-13_4-11del MANE Select | NP_002097.1:n.4-13_4-11del |