HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52492671_52492673delinsGTT , CM000674.2:g.52492671_52492673delinsGTT | GRCh38 |
NC_000012.11:g.52886455_52886457delinsGTT , CM000674.1:g.52886455_52886457delinsGTT | GRCh37 |
NC_000012.10:g.51172722_51172724delinsGTT | NCBI36 |
NG_008298.1:g.5725_5727delinsAAC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000330722.7:c.516_518delinsAAC MANE Select | ENSP00000369317.3:p.Asn172_Lys173delinsLy... | |
ENST00000330722.6:c.516_518delinsAAC | ENSP00000369317.3:p.Asn172_Lys173delinsLy... | |
ENST00000549898.5:n.37_39delinsAAC | ||
NM_005554.3:c.516_518delinsAAC | NP_005545.1:p.Asn172_Lys173delinsLysThr | |
NM_005554.4:c.516_518delinsAAC MANE Select | NP_005545.1:p.Asn172_Lys173delinsLysThr |