HGVS | Genome Assembly |
---|---|
NC_000001.11:g.109264390_109264391insCCCCCCCCCCC , CM000663.2:g.109264390_109264391insCCCCCCCCCCC | GRCh38 |
NC_000001.10:g.109807012_109807013insCCCCCCCCCCC , CM000663.1:g.109807012_109807013insCCCCCCCCCCC | GRCh37 |
NC_000001.9:g.109608535_109608536insCCCCCCCCCCC | NCBI36 |
NG_052669.1:g.19686_19687insCCCCCCCCCCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271332.4:c.5289+25_5289+26insCCCCCCCCCCC MANE Select | ENSP00000271332.3:n.5289+25_5289+26insCCCCCCCCCCC | |
ENST00000271332.3:c.5289+25_5289+26insCCCCCCCCCCC | ENSP00000271332.3:n.5289+25_5289+26insCCCCCCCCCCC | |
NM_001408.2:c.5289+25_5289+26insCCCCCCCCCCC | NP_001399.1:n.5289+25_5289+26insCCCCCCCCCCC | |
XM_005270580.3:c.5289+25_5289+26insCCCCCCCCCCC | XP_005270637.1:n.5289+25_5289+26insCCCCCCCCCCC | |
NM_001408.3:c.5289+25_5289+26insCCCCCCCCCCC MANE Select | NP_001399.1:n.5289+25_5289+26insCCCCCCCCCCC |