HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152675719_152675720delinsTA , CM000669.2:g.152675719_152675720delinsTA | GRCh38 |
NC_000007.13:g.152372804_152372805delinsTA , CM000669.1:g.152372804_152372805delinsTA | GRCh37 |
NC_000007.12:g.152003737_152003738delinsTA | NCBI36 |
NG_027988.1:g.5446_5447delinsTA | |
NG_027988.2:g.5446_5447delinsTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.-48+321_-48+322delinsTA | ENSP00000513758.1:n.-48+321_-48+322delinsTA | |
ENST00000698507.1:n.107+321_107+322delinsTA | ||
ENST00000359321.2:c.39+321_39+322delinsTA MANE Select | ENSP00000352271.1:n.39+321_39+322delinsTA | |
ENST00000359321.1:c.39+321_39+322delinsTA | ENSP00000352271.1:n.39+321_39+322delinsTA | |
NM_005431.1:c.39+321_39+322delinsTA | NP_005422.1:n.39+321_39+322delinsTA | |
NM_005431.2:c.39+321_39+322delinsTA MANE Select | NP_005422.1:n.39+321_39+322delinsTA |