HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1423680_1423682delinsCCT , CM000667.2:g.1423680_1423682delinsCCT | GRCh38 |
NC_000005.9:g.1423795_1423797delinsCCT , CM000667.1:g.1423795_1423797delinsCCT | GRCh37 |
NC_000005.8:g.1476795_1476797delinsCCT | NCBI36 |
NG_015885.1:g.26747_26749delinsAGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.654-1668_654-1666delinsAGG MANE Select | ENSP00000270349.9:n.654-1668_654-1666delinsAGG | |
ENST00000270349.11:c.654-1668_654-1666delinsAGG | ENSP00000270349.9:n.654-1668_654-1666delinsAGG | |
NM_001044.4:c.654-1668_654-1666delinsAGG | NP_001035.1:n.654-1668_654-1666delinsAGG | |
NM_001044.5:c.654-1668_654-1666delinsAGG MANE Select | NP_001035.1:n.654-1668_654-1666delinsAGG |