HGVS | Genome Assembly |
---|---|
NC_000009.12:g.128946071_128946077del , CM000671.2:g.128946071_128946077del | GRCh38 |
NC_000009.11:g.131708350_131708356del , CM000671.1:g.131708350_131708356del | GRCh37 |
NC_000009.10:g.130748171_130748177del | NCBI36 |
NG_017009.1:g.6659_6665del , LRG_744:g.6659_6665del | |
NG_033111.1:g.3379_3385del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372586.4:c.1229_1235del MANE Select | ENSP00000361667.3:p.Tyr410SerfsTer10 | |
ENST00000372586.3:c.1229_1235del | ENSP00000361667.3:p.Tyr410SerfsTer10 | |
ENST00000482796.1:c.39-3118_39-3112del | ENSP00000417556.2:n.39-3118_39-3112del | |
NM_014908.3:c.1229_1235del , LRG_744t1:c.1229_1235del | NP_055723.1:p.Tyr410SerfsTer10 | |
NM_014908.4:c.1229_1235del MANE Select | NP_055723.1:p.Tyr410SerfsTer10 |