HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135303_26135309delinsTATCAAC , CM000664.2:g.26135303_26135309delinsTATCAAC | GRCh38 |
NC_000002.11:g.26358172_26358178delinsTATCAAC , CM000664.1:g.26358172_26358178delinsTATCAAC | GRCh37 |
NC_000002.10:g.26211676_26211682delinsTATCAAC | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*282_*288delinsTATCAAC MANE Select | ENSP00000264710.4:n.*282_*288delinsTATCAAC | |
ENST00000264710.4:c.*282_*288delinsTATCAAC | ENSP00000264710.4:n.*282_*288delinsTATCAAC | |
ENST00000495146.5:n.1248_1254delinsTATCAAC | ||
NM_016131.4:c.*282_*288delinsTATCAAC | NP_057215.3:n.*282_*288delinsTATCAAC | |
XM_024452565.1:c.*282_*288delinsTATCAAC | XP_024308333.1:n.*282_*288delinsTATCAAC | |
NM_016131.5:c.*282_*288delinsTATCAAC MANE Select | NP_057215.3:n.*282_*288delinsTATCAAC |