HGVS | Genome Assembly |
---|---|
NC_000003.12:g.147413316_147413320delinsCTCTT , CM000665.2:g.147413316_147413320delinsCTCTT | GRCh38 |
NC_000003.11:g.147131103_147131107delinsCTCTT , CM000665.1:g.147131103_147131107delinsCTCTT | GRCh37 |
NC_000003.10:g.148613793_148613797delinsCTCTT | NCBI36 |
NG_015886.1:g.8923_8927delinsCTCTT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000282928.5:c.1147-38_1147-34delinsCTCTT MANE Select | ENSP00000282928.4:n.1147-38_1147-34delins... | |
ENST00000282928.4:c.1147-38_1147-34delinsCTCTT | ENSP00000282928.4:n.1147-38_1147-34delins... | |
ENST00000472523.1:n.521+19374_521+19378delinsCTCTT | ||
ENST00000488404.5:c.213-38_213-34delinsCTCTT | ||
NM_003412.3:c.1147-38_1147-34delinsCTCTT | NP_003403.2:n.1147-38_1147-34delinsCTCTT | |
NM_003412.4:c.1147-38_1147-34delinsCTCTT MANE Select | NP_003403.2:n.1147-38_1147-34delinsCTCTT |