HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107212_91107213insGAGAAAG , CM000674.2:g.91107212_91107213insGAGAAAG | GRCh38 |
NC_000012.11:g.91500989_91500990insGAGAAAG , CM000674.1:g.91500989_91500990insGAGAAAG | GRCh37 |
NC_000012.10:g.90025120_90025121insGAGAAAG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.5:c.862+905_862+906insCTTTCTC MANE Select | ENSP00000266718.4:n.862+905_862+906insCTTTCTC | |
ENST00000266718.4:c.862+905_862+906insCTTTCTC | ENSP00000266718.4:n.862+905_862+906insCTTTCTC | |
ENST00000546642.1:n.612+905_612+906insCTTTCTC | ||
ENST00000548071.1:n.255+905_255+906insCTTTCTC | ||
NM_002345.3:c.862+905_862+906insCTTTCTC | NP_002336.1:n.862+905_862+906insCTTTCTC | |
NM_002345.4:c.862+905_862+906insCTTTCTC MANE Select | NP_002336.1:n.862+905_862+906insCTTTCTC |