HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114713915_114713916insGTTATCCAGTATG , CM000663.2:g.114713915_114713916insGTTATCCAGTATG | GRCh38 |
NC_000001.10:g.115256536_115256537insGTTATCCAGTATG , CM000663.1:g.115256536_115256537insGTTATCCAGTATG | GRCh37 |
NC_000001.9:g.115058059_115058060insGTTATCCAGTATG | NCBI36 |
NG_007572.1:g.7979_7980insCATACTGGATAAC , LRG_92:g.7979_7980insCATACTGGATAAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.174_175insCATACTGGATAAC MANE Select | ENSP00000358548.4:p.Ala59HisfsTer4 | |
ENST00000369535.4:c.174_175insCATACTGGATAAC | ENSP00000358548.4:p.Ala59HisfsTer4 | |
NM_002524.4:c.174_175insCATACTGGATAAC | NP_002515.1:p.Ala59HisfsTer4 | |
NM_002524.5:c.174_175insCATACTGGATAAC MANE Select | NP_002515.1:p.Ala59HisfsTer4 |