HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69353496_69353497insTTTTTTTTTTTTTTTTT , CM000674.2:g.69353496_69353497insTTTTTTTTTTTTTTTTT | GRCh38 |
NC_000012.11:g.69747276_69747277insTTTTTTTTTTTTTTTTT , CM000674.1:g.69747276_69747277insTTTTTTTTTTTTTTTTT | GRCh37 |
NC_000012.10:g.68033543_68033544insTTTTTTTTTTTTTTTTT | NCBI36 |
NG_008195.1:g.10143_10144insTTTTTTTTTTTTTTTTT , LRG_768:g.10143_10144insTTTTTTTTTTTTTTTTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261267.7:c.*277_*278insTTTTTTTTTTTTTTTTT MANE Select | ENSP00000261267.2:n.*277_*278insTTTTTTTTTTTTTTTTT | |
ENST00000261267.6:c.*277_*278insTTTTTTTTTTTTTTTTT | ENSP00000261267.2:n.*277_*278insTTTTTTTTTTTTTTTTT | |
NM_000239.2:c.*277_*278insTTTTTTTTTTTTTTTTT , LRG_768t1:c.*277_*278insTTTTTTTTTTTTTTTTT | NP_000230.1:n.*277_*278insTTTTTTTTTTTTTTTTT | |
NM_000239.3:c.*277_*278insTTTTTTTTTTTTTTTTT MANE Select | NP_000230.1:n.*277_*278insTTTTTTTTTTTTTTTTT |