HGVS | Genome Assembly |
---|---|
NC_000019.10:g.9214441_9214442insTG , CM000681.2:g.9214441_9214442insTG | GRCh38 |
NC_000019.9:g.9325117_9325118insTG , CM000681.1:g.9325117_9325118insTG | GRCh37 |
NC_000019.8:g.9186117_9186118insTG | NCBI36 |
NG_027953.1:g.5430_5431insCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000641244.1:c.396_397insCA | ENSP00000493404.1:p.Thr133GlnfsTer5 | |
ENST00000641669.1:c.396_397insCA MANE Select | ENSP00000493383.1:p.Thr133GlnfsTer5 | |
ENST00000308682.3:c.396_397insCA | ENSP00000310488.2:p.Thr133GlnfsTer5 | |
NM_001005191.2:c.396_397insCA | NP_001005191.1:p.Thr133GlnfsTer5 | |
NM_001005191.3:c.396_397insCA MANE Select | NP_001005191.1:p.Thr133GlnfsTer5 |