HGVS | Genome Assembly |
---|---|
NC_000020.11:g.44651895_44651896insTC , CM000682.2:g.44651895_44651896insTC | GRCh38 |
NC_000020.10:g.43280536_43280537insTC , CM000682.1:g.43280536_43280537insTC | GRCh37 |
NC_000020.9:g.42713950_42713951insTC | NCBI36 |
NG_007385.1:g.4840_4841insGA , LRG_16:g.4840_4841insGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000536076.2:c.-121+6_-121+7insGA | ENSP00000512234.1:n.-121+6_-121+7insGA | |
ENST00000696039.1:n.321+6_321+7insGA | ||
ENST00000696062.1:c.96+204_96+205insGA | ENSP00000512365.1:n.96+204_96+205insGA | |
ENST00000696064.1:c.-118+6_-118+7insGA | ENSP00000512367.1:n.-118+6_-118+7insGA | |
ENST00000696065.1:c.-121+6_-121+7insGA | ENSP00000512368.1:n.-121+6_-121+7insGA | |
ENST00000535573.1:n.332+6_332+7insGA | ||
ENST00000536076.1:n.213+6_213+7insGA | ||
XM_011528479.1:c.-257+6_-257+7insGA | XP_011526781.1:n.-257+6_-257+7insGA |