HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24278038_24278040delinsAAC , CM000668.2:g.24278038_24278040delinsAAC | GRCh38 |
NC_000006.11:g.24278266_24278268delinsAAC , CM000668.1:g.24278266_24278268delinsAAC | GRCh37 |
NC_000006.10:g.24386245_24386247delinsAAC | NCBI36 |
NG_012829.1:g.85013_85015delinsGTT | |
NG_012829.2:g.110253_110255delinsGTT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378454.8:c.922+9_922+11delinsGTT MANE Select | ENSP00000367715.3:n.922+9_922+11delinsGTT | |
ENST00000378454.7:c.922+9_922+11delinsGTT | ENSP00000367715.3:n.922+9_922+11delinsGTT | |
NM_001195610.1:c.922+9_922+11delinsGTT | NP_001182539.1:n.922+9_922+11delinsGTT | |
NM_016356.4:c.922+9_922+11delinsGTT | NP_057440.2:n.922+9_922+11delinsGTT | |
NM_016356.5:c.922+9_922+11delinsGTT MANE Select | NP_057440.2:n.922+9_922+11delinsGTT | |
NM_001195610.2:c.922+9_922+11delinsGTT | NP_001182539.1:n.922+9_922+11delinsGTT |