HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322873_73322899del , CM000677.2:g.73322873_73322899del | GRCh38 |
NC_000015.9:g.73615214_73615240del , CM000677.1:g.73615214_73615240del | GRCh37 |
NC_000015.8:g.71402267_71402293del | NCBI36 |
NG_009063.1:g.51368_51394del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261917.4:c.3196_3222del MANE Select | ENSP00000261917.3:p.Pro1066_Leu1074del | |
ENST00000261917.3:c.3196_3222del | ENSP00000261917.3:p.Pro1066_Leu1074del | |
NM_005477.2:c.3196_3222del | NP_005468.1:p.Pro1066_Leu1074del | |
XM_011521148.1:c.1978_2004del | XP_011519450.1:p.Pro660_Leu668del | |
XM_011521148.2:c.1978_2004del | XP_011519450.1:p.Pro660_Leu668del | |
NM_005477.3:c.3196_3222del MANE Select | NP_005468.1:p.Pro1066_Leu1074del |