HGVS | Genome Assembly |
---|---|
NC_000023.11:g.108084508_108084509delinsTA , CM000685.2:g.108084508_108084509delinsTA | GRCh38 |
NC_000023.10:g.107327738_107327739delinsTA , CM000685.1:g.107327738_107327739delinsTA | GRCh37 |
NC_000023.9:g.107214394_107214395delinsTA | NCBI36 |
NG_012521.1:g.12110_12111delinsTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217958.8:c.*465_*466delinsTA MANE Select | ENSP00000217958.3:n.*465_*466delinsTA | |
ENST00000217958.7:c.*465_*466delinsTA | ENSP00000217958.3:n.*465_*466delinsTA | |
NM_002814.3:c.*465_*466delinsTA | NP_002805.1:n.*465_*466delinsTA | |
NM_170750.2:c.*611_*612delinsTA | NP_736606.1:n.*611_*612delinsTA | |
NM_002814.4:c.*465_*466delinsTA MANE Select | NP_002805.1:n.*465_*466delinsTA | |
NM_170750.3:c.*611_*612delinsTA | NP_736606.1:n.*611_*612delinsTA |