HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5225824_5225825delinsGA , CM000673.2:g.5225824_5225825delinsGA | GRCh38 |
NC_000011.9:g.5247054_5247055delinsGA , CM000673.1:g.5247054_5247055delinsGA | GRCh37 |
NC_000011.8:g.5203630_5203631delinsGA | NCBI36 |
NG_000007.3:g.71791_71792delinsTC | |
NG_059281.1:g.6247_6248delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647020.1:c.316-99_316-98delinsTC | ENSP00000494175.1:n.316-99_316-98delinsTC | |
ENST00000335295.4:c.316-99_316-98delinsTC MANE Select | ENSP00000333994.3:n.316-99_316-98delinsTC | |
ENST00000475226.1:n.248-99_248-98delinsTC | ||
ENST00000633227.1:c.*132-99_*132-98delinsTC | ENSP00000488004.1:n.*132-99_*132-98delinsTC | |
NM_000518.4:c.316-99_316-98delinsTC | NP_000509.1:n.316-99_316-98delinsTC | |
NM_000518.5:c.316-99_316-98delinsTC MANE Select | NP_000509.1:n.316-99_316-98delinsTC |