HGVS | Genome Assembly |
---|---|
NC_000001.11:g.10972957_10972958insT , CM000663.2:g.10972957_10972958insT | GRCh38 |
NC_000001.10:g.11033014_11033015insT , CM000663.1:g.11033014_11033015insT | GRCh37 |
NC_000001.9:g.10955601_10955602insT | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000377004.9:c.128-2869_128-2868insA MANE Select | ENSP00000366203.4:n.128-2869_128-2868insA... | |
ENST00000377004.8:c.128-2869_128-2868insA | ENSP00000366203.4:n.128-2869_128-2868insA... | |
ENST00000520253.1:c.61-2869_61-2868insA | ||
NM_001170754.1:c.128-2869_128-2868insA | NP_001164225.1:n.128-2869_128-2868insA | |
NM_001170754.2:c.128-2869_128-2868insA MANE Select | NP_001164225.1:n.128-2869_128-2868insA |