HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94852628_94852632del , CM000672.2:g.94852628_94852632del | GRCh38 |
NC_000010.10:g.96612385_96612389del , CM000672.1:g.96612385_96612389del | GRCh37 |
NC_000010.9:g.96602375_96602379del | NCBI36 |
NG_008384.2:g.94923_94927del | |
NG_008384.3:g.94948_94952del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.1292-105_1292-101del MANE Select | ENSP00000360372.3:n.1292-105_1292-101del | |
ENST00000645461.1:n.2203-105_2203-101del | ||
ENST00000371321.7:c.1292-105_1292-101del | ENSP00000360372.3:n.1292-105_1292-101del | |
ENST00000464755.1:c.2055-105_2055-101del | ENSP00000483243.1:n.2055-105_2055-101del | |
NM_000769.2:c.1292-105_1292-101del | NP_000760.1:n.1292-105_1292-101del | |
NM_000769.4:c.1292-105_1292-101del MANE Select | NP_000760.1:n.1292-105_1292-101del |