HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135187_26135189delinsCTT , CM000664.2:g.26135187_26135189delinsCTT | GRCh38 |
NC_000002.11:g.26358056_26358058delinsCTT , CM000664.1:g.26358056_26358058delinsCTT | GRCh37 |
NC_000002.10:g.26211560_26211562delinsCTT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*166_*168delinsCTT MANE Select | ENSP00000264710.4:n.*166_*168delinsCTT | |
ENST00000264710.4:c.*166_*168delinsCTT | ENSP00000264710.4:n.*166_*168delinsCTT | |
ENST00000495146.5:n.1132_1134delinsCTT | ||
NM_016131.4:c.*166_*168delinsCTT | NP_057215.3:n.*166_*168delinsCTT | |
XM_024452565.1:c.*166_*168delinsCTT | XP_024308333.1:n.*166_*168delinsCTT | |
NM_016131.5:c.*166_*168delinsCTT MANE Select | NP_057215.3:n.*166_*168delinsCTT |