HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107225_91107238delinsGA , CM000674.2:g.91107225_91107238delinsGA | GRCh38 |
NC_000012.11:g.91501002_91501015delinsGA , CM000674.1:g.91501002_91501015delinsGA | GRCh37 |
NC_000012.10:g.90025133_90025146delinsGA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.5:c.862+880_862+893delinsTC MANE Select | ENSP00000266718.4:n.862+880_862+893delinsTC | |
ENST00000266718.4:c.862+880_862+893delinsTC | ENSP00000266718.4:n.862+880_862+893delinsTC | |
ENST00000546642.1:n.612+880_612+893delinsTC | ||
ENST00000548071.1:n.255+880_255+893delinsTC | ||
NM_002345.3:c.862+880_862+893delinsTC | NP_002336.1:n.862+880_862+893delinsTC | |
NM_002345.4:c.862+880_862+893delinsTC MANE Select | NP_002336.1:n.862+880_862+893delinsTC |