HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19957794_19957796delinsTTA , CM000670.2:g.19957794_19957796delinsTTA | GRCh38 |
NC_000008.10:g.19815305_19815307delinsTTA , CM000670.1:g.19815305_19815307delinsTTA | GRCh37 |
NC_000008.9:g.19859585_19859587delinsTTA | NCBI36 |
NG_008855.1:g.23724_23726delinsTTA | |
NG_008855.2:g.61078_61080delinsTTA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.1019-1466_1019-1464delinsTTA MANE Select | ENSP00000497642.1:n.1019-1466_1019-1464delinsTTA | |
ENST00000650478.1:c.79+1711_79+1713delinsTTA | ENSP00000497560.1:n.79+1711_79+1713delinsTTA | |
ENST00000311322.8:c.1019-1466_1019-1464delinsTTA | ENSP00000309757.6:n.1019-1466_1019-1464delinsTTA | |
NM_000237.2:c.1019-1466_1019-1464delinsTTA | NP_000228.1:n.1019-1466_1019-1464delinsTTA | |
NM_000237.3:c.1019-1466_1019-1464delinsTTA MANE Select | NP_000228.1:n.1019-1466_1019-1464delinsTTA |