HGVS | Genome Assembly |
---|---|
NC_000007.14:g.37906682_37906686delinsCCTAA , CM000669.2:g.37906682_37906686delinsCCTAA | GRCh38 |
NC_000007.13:g.37946284_37946288delinsCCTAA , CM000669.1:g.37946284_37946288delinsCCTAA | GRCh37 |
NC_000007.12:g.37912809_37912813delinsCCTAA | NCBI36 |
NG_052980.1:g.15238_15242delinsTTAGG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000436072.7:c.*793_*797delinsTTAGG (SFRP4) MANE Select | ENSP00000410715.2:n.*793_*797delinsTTAGG | |
ENST00000436072.6:c.*793_*797delinsTTAGG (SFRP4) | ENSP00000410715.2:n.*793_*797delinsTTAGG | |
ENST00000476620.1:c.-37-42158_-37-42154delinsCCTAA (EPDR1) | ENSP00000425858.1:n.-37-42158_-37-42154de... | |
NM_003014.3:c.*793_*797delinsTTAGG (SFRP4) | NP_003005.2:n.*793_*797delinsTTAGG | |
NM_003014.4:c.*793_*797delinsTTAGG (SFRP4) MANE Select | NP_003005.2:n.*793_*797delinsTTAGG |