HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8732023_8732024delinsAC , CM000685.2:g.8732023_8732024delinsAC | GRCh38 |
NC_000023.10:g.8700064_8700065delinsAC , CM000685.1:g.8700064_8700065delinsAC | GRCh37 |
NC_000023.9:g.8660064_8660065delinsAC | NCBI36 |
NG_007088.1:g.5163_5164delinsGT | |
NG_007088.2:g.5163_5164delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262648.8:c.13_14delinsGT MANE Select | ENSP00000262648.3:p.Val5= | |
ENST00000262648.7:c.13_14delinsGT | ENSP00000262648.3:p.Val5= | |
ENST00000619786.1:c.13_14delinsGT | ENSP00000478734.1:p.Val5= | |
NM_000216.2:c.13_14delinsGT | NP_000207.2:p.Val5= | |
XM_005274501.3:c.13_14delinsGT | XP_005274558.1:p.Val5= | |
NM_000216.3:c.13_14delinsGT | NP_000207.2:p.Val5= | |
XM_005274501.4:c.13_14delinsGT | XP_005274558.1:p.Val5= | |
NM_000216.4:c.13_14delinsGT MANE Select | NP_000207.2:p.Val5= |