HGVS | Genome Assembly |
---|---|
NC_000012.12:g.71941939_71941941delinsCAG , CM000674.2:g.71941939_71941941delinsCAG | GRCh38 |
NC_000012.11:g.72335719_72335721delinsCAG , CM000674.1:g.72335719_72335721delinsCAG | GRCh37 |
NC_000012.10:g.70621986_70621988delinsCAG | NCBI36 |
NG_008279.1:g.8094_8096delinsCAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000333850.4:c.255+206_255+208delinsCAG MANE Select | ENSP00000329093.3:n.255+206_255+208delinsCAG | |
ENST00000333850.3:c.255+206_255+208delinsCAG | ENSP00000329093.3:n.255+206_255+208delinsCAG | |
ENST00000546576.1:n.265+206_265+208delinsCAG | ||
NM_173353.3:c.255+206_255+208delinsCAG | NP_775489.2:n.255+206_255+208delinsCAG | |
XR_245894.2:n.355+206_355+208delinsCAG | ||
XR_001748575.1:n.355+206_355+208delinsCAG | ||
NM_173353.4:c.255+206_255+208delinsCAG MANE Select | NP_775489.2:n.255+206_255+208delinsCAG |