HGVS | Genome Assembly |
---|---|
NC_000012.12:g.120737094_120737096delinsTGC , CM000674.2:g.120737094_120737096delinsTGC | GRCh38 |
NC_000012.11:g.121174897_121174899delinsTGC , CM000674.1:g.121174897_121174899delinsTGC | GRCh37 |
NC_000012.10:g.119659280_119659282delinsTGC | NCBI36 |
NG_007991.1:g.16327_16329delinsTGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242592.9:c.319_321delinsTGC MANE Select | ENSP00000242592.4:p.Arg107Cys | |
ENST00000242592.8:c.319_321delinsTGC | ENSP00000242592.4:p.Arg107Cys | |
ENST00000411593.2:c.319_321delinsTGC | ENSP00000401045.2:p.Arg107Cys | |
ENST00000539690.1:n.431_433delinsTGC | ||
NM_000017.3:c.319_321delinsTGC | NP_000008.1:p.Arg107Cys | |
NM_001302554.1:c.319_321delinsTGC | NP_001289483.1:p.Arg107Cys | |
NM_000017.4:c.319_321delinsTGC MANE Select | NP_000008.1:p.Arg107Cys | |
NM_001302554.2:c.319_321delinsTGC | NP_001289483.1:p.Arg107Cys |