HGVS | Genome Assembly |
---|---|
NC_000017.11:g.82727236_82727242del , CM000679.2:g.82727236_82727242del | GRCh38 |
NC_000017.10:g.80685112_80685118del , CM000679.1:g.80685112_80685118del | GRCh37 |
NC_000017.9:g.78278401_78278407del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269373.11:c.*65_*71del MANE Select | ENSP00000269373.6:n.*65_*71del | |
ENST00000269373.10:c.*65_*71del | ENSP00000269373.6:n.*65_*71del | |
ENST00000571594.1:c.53+69_53+75del | ENSP00000459751.1:n.53+69_53+75del | |
ENST00000574832.5:c.*952_*958del | ENSP00000460869.1:n.*952_*958del | |
NM_024619.3:c.*65_*71del | NP_078895.2:n.*65_*71del | |
NR_046408.1:n.1173_1179del | ||
XM_024450948.1:c.*65_*71del | XP_024306716.1:n.*65_*71del | |
NM_024619.4:c.*65_*71del MANE Select | NP_078895.2:n.*65_*71del | |
NR_046408.2:n.1173_1179del |