HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107367_91107369delinsGAA , CM000674.2:g.91107367_91107369delinsGAA | GRCh38 |
NC_000012.11:g.91501144_91501146delinsGAA , CM000674.1:g.91501144_91501146delinsGAA | GRCh37 |
NC_000012.10:g.90025275_90025277delinsGAA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.5:c.862+749_862+751delinsTTC MANE Select | ENSP00000266718.4:n.862+749_862+751delinsTTC | |
ENST00000266718.4:c.862+749_862+751delinsTTC | ENSP00000266718.4:n.862+749_862+751delinsTTC | |
ENST00000546642.1:n.612+749_612+751delinsTTC | ||
ENST00000548071.1:n.255+749_255+751delinsTTC | ||
NM_002345.3:c.862+749_862+751delinsTTC | NP_002336.1:n.862+749_862+751delinsTTC | |
NM_002345.4:c.862+749_862+751delinsTTC MANE Select | NP_002336.1:n.862+749_862+751delinsTTC |