HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135209_26135210delinsCA , CM000664.2:g.26135209_26135210delinsCA | GRCh38 |
NC_000002.11:g.26358078_26358079delinsCA , CM000664.1:g.26358078_26358079delinsCA | GRCh37 |
NC_000002.10:g.26211582_26211583delinsCA | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264710.5:c.*188_*189delinsCA MANE Select | ENSP00000264710.4:n.*188_*189delinsCA | |
ENST00000264710.4:c.*188_*189delinsCA | ENSP00000264710.4:n.*188_*189delinsCA | |
ENST00000495146.5:n.1154_1155delinsCA | ||
NM_016131.4:c.*188_*189delinsCA | NP_057215.3:n.*188_*189delinsCA | |
XM_024452565.1:c.*188_*189delinsCA | XP_024308333.1:n.*188_*189delinsCA | |
NM_016131.5:c.*188_*189delinsCA MANE Select | NP_057215.3:n.*188_*189delinsCA |