HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215728232_215728234dup , CM000663.2:g.215728232_215728234dup | GRCh38 |
NC_000001.10:g.215901574_215901576dup , CM000663.1:g.215901574_215901576dup | GRCh37 |
NC_000001.9:g.213968197_213968199dup | NCBI36 |
NG_009497.1:g.700165_700167dup | |
NG_009497.2:g.700217_700219dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.11864_11866dup MANE Select | ENSP00000305941.3:p.Trp3955_Ser3956insTrp | |
ENST00000674083.1:c.11864_11866dup | ENSP00000501296.1:p.Trp3955_Ser3956insTrp | |
ENST00000307340.7:c.11864_11866dup | ENSP00000305941.3:p.Trp3955_Ser3956insTrp | |
NM_206933.2:c.11864_11866dup | NP_996816.2:p.Trp3955_Ser3956insTrp | |
NM_206933.3:c.11864_11866dup | NP_996816.2:p.Trp3955_Ser3956insTrp | |
NM_206933.4:c.11864_11866dup MANE Select | NP_996816.3:p.Trp3955_Ser3956insTrp |