HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19961713_19961714delinsAG , CM000670.2:g.19961713_19961714delinsAG | GRCh38 |
NC_000008.10:g.19819224_19819225delinsAG , CM000670.1:g.19819224_19819225delinsAG | GRCh37 |
NC_000008.9:g.19863504_19863505delinsAG | NCBI36 |
NG_008855.1:g.27643_27644delinsAG | |
NG_008855.2:g.64997_64998delinsAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.1323-402_1323-401delinsAG MANE Select | ENSP00000497642.1:n.1323-402_1323-401delinsAG | |
ENST00000650478.1:c.263-402_263-401delinsAG | ENSP00000497560.1:n.263-402_263-401delinsAG | |
ENST00000311322.8:c.1323-402_1323-401delinsAG | ENSP00000309757.6:n.1323-402_1323-401delinsAG | |
NM_000237.2:c.1323-402_1323-401delinsAG | NP_000228.1:n.1323-402_1323-401delinsAG | |
NM_000237.3:c.1323-402_1323-401delinsAG MANE Select | NP_000228.1:n.1323-402_1323-401delinsAG |