HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140114585_140114614delinsCGCAGGACGAGCCGCGCCGGGCGCTCAAAA , CM000667.2:g.140114585_140114614delinsCGCAGGACGAGCCGCGCCGGGCGCTCAAAA | GRCh38 |
NC_000005.9:g.139494170_139494199delinsCGCAGGACGAGCCGCGCCGGGCGCTCAAAA , CM000667.1:g.139494170_139494199delinsCGCAGGACGAGCCGCGCCGGGCGCTCAAAA | GRCh37 |
NC_000005.8:g.139474354_139474383delinsCGCAGGACGAGCCGCGCCGGGCGCTCAAAA | NCBI36 |
NG_041813.1:g.5463_5492delinsCGCAGGACGAGCCGCGCCGGGCGCTCAAAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331327.5:c.404_433delinsCGCAGGACGAGCCGCGCCGGGCGCTCAAAA MANE Select | ENSP00000332706.3:p.Ala135= | |
ENST00000651386.1:c.404_433delinsCGCAGGACGAGCCGCGCCGGGCGCTCAAAA | ENSP00000499133.1:p.Ala135= | |
ENST00000331327.4:c.404_433delinsCGCAGGACGAGCCGCGCCGGGCGCTCAAAA | ENSP00000332706.3:p.Ala135= | |
NM_005859.4:c.404_433delinsCGCAGGACGAGCCGCGCCGGGCGCTCAAAA | NP_005850.1:p.Ala135= | |
NM_005859.5:c.404_433delinsCGCAGGACGAGCCGCGCCGGGCGCTCAAAA MANE Select | NP_005850.1:p.Ala135= |