HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55110571_55110572delinsGA , CM000666.2:g.55110571_55110572delinsGA | GRCh38 |
NC_000004.11:g.55976738_55976739delinsGA , CM000666.1:g.55976738_55976739delinsGA | GRCh37 |
NC_000004.10:g.55671495_55671496delinsGA | NCBI36 |
NG_012004.1:g.20024_20025delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.1092-6_1092-5delinsTC MANE Select | ENSP00000263923.4:n.1092-6_1092-5delinsTC | |
ENST00000647068.1:n.1105-6_1105-5delinsTC | ||
ENST00000263923.4:c.1092-6_1092-5delinsTC | ENSP00000263923.4:n.1092-6_1092-5delinsTC | |
ENST00000512566.1:n.1092-6_1092-5delinsTC | ||
NM_002253.2:c.1092-6_1092-5delinsTC | NP_002244.1:n.1092-6_1092-5delinsTC | |
NM_002253.3:c.1092-6_1092-5delinsTC | NP_002244.1:n.1092-6_1092-5delinsTC | |
NM_002253.4:c.1092-6_1092-5delinsTC MANE Select | NP_002244.1:n.1092-6_1092-5delinsTC |