HGVS | Genome Assembly |
---|---|
NC_000010.11:g.17129757_17129759dup , CM000672.2:g.17129757_17129759dup | GRCh38 |
NC_000010.10:g.17171756_17171758dup , CM000672.1:g.17171756_17171758dup | GRCh37 |
NC_000010.9:g.17211762_17211764dup | NCBI36 |
NG_008967.1:g.5060_5062dup , LRG_540:g.5060_5062dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377833.10:c.8_10dup MANE Select | ENSP00000367064.4:p.Asn3_Met4insAsn | |
ENST00000377823.1:c.8_10dup | ENSP00000367054.1:p.Asn3_Met4insAsn | |
ENST00000377833.8:c.8_10dup | ENSP00000367064.4:p.Asn3_Met4insAsn | |
NM_001081.3:c.8_10dup , LRG_540t1:c.8_10dup | NP_001072.2:p.Asn3_Met4insAsn | |
XM_011519708.1:c.8_10dup | XP_011518010.1:p.Asn3_Met4insAsn | |
XM_011519708.2:c.8_10dup | XP_011518010.1:p.Asn3_Met4insAsn | |
NM_001081.4:c.8_10dup MANE Select | NP_001072.2:p.Asn3_Met4insAsn |