HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154904082_154904083del , CM000685.2:g.154904082_154904083del | GRCh38 |
NC_000023.10:g.154132357_154132358del , CM000685.1:g.154132357_154132358del | GRCh37 |
NC_000023.9:g.153785551_153785552del | NCBI36 |
NG_011403.1:g.123641_123642del | |
NG_011403.2:g.123641_123642del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.5821_5822del MANE Select | ENSP00000353393.4:p.Asn1941TrpfsTer29 | |
ENST00000360256.8:c.5821_5822del | ENSP00000353393.4:p.Asn1941TrpfsTer29 | |
NM_000132.3:c.5821_5822del | NP_000123.1:p.Asn1941TrpfsTer29 | |
XM_011531126.1:c.5716_5717del | XP_011529428.1:p.Asn1906TrpfsTer29 | |
NM_000132.4:c.5821_5822del MANE Select | NP_000123.1:p.Asn1941TrpfsTer29 |