HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135299_26135301delinsTTC , CM000664.2:g.26135299_26135301delinsTTC | GRCh38 |
NC_000002.11:g.26358168_26358170delinsTTC , CM000664.1:g.26358168_26358170delinsTTC | GRCh37 |
NC_000002.10:g.26211672_26211674delinsTTC | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264710.5:c.*278_*280delinsTTC MANE Select | ENSP00000264710.4:n.*278_*280delinsTTC | |
ENST00000264710.4:c.*278_*280delinsTTC | ENSP00000264710.4:n.*278_*280delinsTTC | |
ENST00000495146.5:n.1244_1246delinsTTC | ||
NM_016131.4:c.*278_*280delinsTTC | NP_057215.3:n.*278_*280delinsTTC | |
XM_024452565.1:c.*278_*280delinsTTC | XP_024308333.1:n.*278_*280delinsTTC | |
NM_016131.5:c.*278_*280delinsTTC MANE Select | NP_057215.3:n.*278_*280delinsTTC |