HGVS | Genome Assembly |
---|---|
NC_000002.12:g.73641080_73641081insCTAAATAAATATTTGTTTCATTTGGTGGTTGTTCTTATGCAACATTATCCTGGCACTAGAAAAAT , CM000664.2:g.73641080_73641081insCTAAATAAATATTTGTTTCATTTGGTGGTTGTTCTTATGCAACATTATCCTGGCACTAGAAAAAT | GRCh38 |
NC_000002.11:g.73868207_73868208insCTAAATAAATATTTGTTTCATTTGGTGGTTGTTCTTATGCAACATTATCCTGGCACTAGAAAAAT , CM000664.1:g.73868207_73868208insCTAAATAAATATTTGTTTCATTTGGTGGTTGTTCTTATGCAACATTATCCTGGCACTAGAAAAAT | GRCh37 |
NC_000002.10:g.73721715_73721716insCTAAATAAATATTTGTTTCATTTGGTGGTTGTTCTTATGCAACATTATCCTGGCACTAGAAAAAT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272425.4:c.548_549insATTTTTCTAGTGCCAGGATAATGTTGCATAAGAACAACCACCAAATGAAACAAATATTTATTTAG MANE Select | ENSP00000272425.3:p.Ala184PhefsTer3 | |
ENST00000272425.3:c.548_549insATTTTTCTAGTGCCAGGATAATGTTGCATAAGAACAACCACCAAATGAAACAAATATTTATTTAG | ENSP00000272425.3:p.Ala184PhefsTer3 | |
NM_003960.3:c.548_549insATTTTTCTAGTGCCAGGATAATGTTGCATAAGAACAACCACCAAATGAAACAAATATTTATTTAG | NP_003951.3:p.Ala184PhefsTer3 | |
NM_003960.4:c.548_549insATTTTTCTAGTGCCAGGATAATGTTGCATAAGAACAACCACCAAATGAAACAAATATTTATTTAG MANE Select | NP_003951.3:p.Ala184PhefsTer3 |