HGVS | Genome Assembly |
---|---|
NC_000008.11:g.37966087_37966089delinsAGG , CM000670.2:g.37966087_37966089delinsAGG | GRCh38 |
NC_000008.10:g.37823605_37823607delinsAGG , CM000670.1:g.37823605_37823607delinsAGG | GRCh37 |
NC_000008.9:g.37942762_37942764delinsAGG | NCBI36 |
NG_011936.1:g.5578_5580delinsCCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000345060.5:c.381_383delinsCCT MANE Select | ENSP00000343782.3:p.Thr127= | |
ENST00000520341.2:n.509_511delinsCCT | ||
ENST00000345060.4:c.381_383delinsCCT | ENSP00000343782.3:p.Thr127= | |
ENST00000614635.1:c.381_383delinsCCT | ENSP00000480325.1:p.Thr127= | |
NM_000025.2:c.381_383delinsCCT | NP_000016.1:p.Thr127= | |
NM_000025.3:c.381_383delinsCCT MANE Select | NP_000016.1:p.Thr127= |