HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1610702_1610703insTA , CM000668.2:g.1610702_1610703insTA | GRCh38 |
NC_000006.11:g.1610937_1610938insTA , CM000668.1:g.1610937_1610938insTA | GRCh37 |
NC_000006.10:g.1555936_1555937insTA | NCBI36 |
NG_009368.1:g.5257_5258insTA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000645831.2:c.257_258insTA MANE Select | ENSP00000493906.1:p.Ile87ThrfsTer16 | |
ENST00000380874.3:c.257_258insTA | ENSP00000370256.2:p.Ile87ThrfsTer16 | |
NM_001453.2:c.257_258insTA | NP_001444.2:p.Ile87ThrfsTer16 | |
NM_001453.3:c.257_258insTA MANE Select | NP_001444.2:p.Ile87ThrfsTer16 |