HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215817358_215817359insA , CM000663.2:g.215817358_215817359insA | GRCh38 |
NC_000001.10:g.215990700_215990701insA , CM000663.1:g.215990700_215990701insA | GRCh37 |
NC_000001.9:g.214057323_214057324insA | NCBI36 |
NG_009497.1:g.611038_611039insT | |
NG_009497.2:g.611090_611091insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.9372-164_9372-163insT MANE Select | ENSP00000305941.3:n.9372-164_9372-163insT | |
ENST00000674083.1:c.9372-164_9372-163insT | ENSP00000501296.1:n.9372-164_9372-163insT | |
ENST00000307340.7:c.9372-164_9372-163insT | ENSP00000305941.3:n.9372-164_9372-163insT | |
NM_206933.2:c.9372-164_9372-163insT | NP_996816.2:n.9372-164_9372-163insT | |
NM_206933.3:c.9372-164_9372-163insT | NP_996816.2:n.9372-164_9372-163insT | |
NM_206933.4:c.9372-164_9372-163insT MANE Select | NP_996816.3:n.9372-164_9372-163insT |