HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94852590_94852594del , CM000672.2:g.94852590_94852594del | GRCh38 |
NC_000010.10:g.96612347_96612351del , CM000672.1:g.96612347_96612351del | GRCh37 |
NC_000010.9:g.96602337_96602341del | NCBI36 |
NG_008384.2:g.94885_94889del | |
NG_008384.3:g.94910_94914del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.1292-143_1292-139del MANE Select | ENSP00000360372.3:n.1292-143_1292-139del | |
ENST00000645461.1:n.2203-143_2203-139del | ||
ENST00000371321.7:c.1292-143_1292-139del | ENSP00000360372.3:n.1292-143_1292-139del | |
ENST00000464755.1:c.2055-143_2055-139del | ENSP00000483243.1:n.2055-143_2055-139del | |
NM_000769.2:c.1292-143_1292-139del | NP_000760.1:n.1292-143_1292-139del | |
NM_000769.4:c.1292-143_1292-139del MANE Select | NP_000760.1:n.1292-143_1292-139del |