HGVS | Genome Assembly |
---|---|
NC_000012.12:g.71942891_71942892delinsCA , CM000674.2:g.71942891_71942892delinsCA | GRCh38 |
NC_000012.11:g.72336671_72336672delinsCA , CM000674.1:g.72336671_72336672delinsCA | GRCh37 |
NC_000012.10:g.70622938_70622939delinsCA | NCBI36 |
NG_008279.1:g.9046_9047delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333850.4:c.255+1158_255+1159delinsCA MANE Select | ENSP00000329093.3:n.255+1158_255+1159delinsCA | |
ENST00000333850.3:c.255+1158_255+1159delinsCA | ENSP00000329093.3:n.255+1158_255+1159delinsCA | |
ENST00000546576.1:n.265+1158_265+1159delinsCA | ||
NM_173353.3:c.255+1158_255+1159delinsCA | NP_775489.2:n.255+1158_255+1159delinsCA | |
XR_245894.2:n.355+1158_355+1159delinsCA | ||
XR_001748575.1:n.355+1158_355+1159delinsCA | ||
NM_173353.4:c.255+1158_255+1159delinsCA MANE Select | NP_775489.2:n.255+1158_255+1159delinsCA |