HGVS | Genome Assembly |
---|---|
NC_000011.10:g.66560736_66560742delinsTCAACAC , CM000673.2:g.66560736_66560742delinsTCAACAC | GRCh38 |
NC_000011.9:g.66328207_66328213delinsTCAACAC , CM000673.1:g.66328207_66328213delinsTCAACAC | GRCh37 |
NC_000011.8:g.66084783_66084789delinsTCAACAC | NCBI36 |
NG_013304.2:g.18817_18823delinsTCAACAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000513398.2:c.1841_1847delinsTCAACAC MANE Select | ENSP00000426797.1:p.Ile614= | |
ENST00000502692.5:c.1970_1976delinsTCAACAC | ENSP00000422007.1:p.Ile657= | |
ENST00000513398.1:c.1841_1847delinsTCAACAC | ENSP00000426797.1:p.Ile614= | |
NM_001104.3:c.1841_1847delinsTCAACAC | NP_001095.2:p.Ile614= | |
NM_001258371.2:c.1970_1976delinsTCAACAC | NP_001245300.2:p.Ile657= | |
NM_001104.4:c.1841_1847delinsTCAACAC MANE Select | NP_001095.2:p.Ile614= | |
NM_001258371.3:c.1970_1976delinsTCAACAC | NP_001245300.2:p.Ile657= |