HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65246913_65246914insAGAGC , CM000674.2:g.65246913_65246914insAGAGC | GRCh38 |
NC_000012.11:g.65640693_65640694insAGAGC , CM000674.1:g.65640693_65640694insAGAGC | GRCh37 |
NC_000012.10:g.63926960_63926961insAGAGC | NCBI36 |
NG_016210.1:g.82343_82344insAGAGC | |
NG_016210.2:g.82343_82344insAGAGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.*588_*589insAGAGC MANE Select | ENSP00000308369.2:n.*588_*589insAGAGC | |
ENST00000308330.2:c.*588_*589insAGAGC | ENSP00000308369.2:n.*588_*589insAGAGC | |
NM_001167614.1:c.*588_*589insAGAGC | NP_001161086.1:n.*588_*589insAGAGC | |
NM_014319.4:c.*588_*589insAGAGC | NP_055134.2:n.*588_*589insAGAGC | |
NM_014319.5:c.*588_*589insAGAGC MANE Select | NP_055134.2:n.*588_*589insAGAGC | |
NM_001167614.2:c.*588_*589insAGAGC | NP_001161086.1:n.*588_*589insAGAGC |