HGVS | Genome Assembly |
---|---|
NC_000010.11:g.103086423_103086424delinsTG , CM000672.2:g.103086423_103086424delinsTG | GRCh38 |
NC_000010.10:g.104846180_104846181delinsTG , CM000672.1:g.104846180_104846181delinsTG | GRCh37 |
NC_000010.9:g.104836170_104836171delinsTG | NCBI36 |
NG_042272.1:g.111883_111884delinsCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369878.9:c.*9243_*9244delinsTG MANE Select | ENSP00000358894.3:n.*9243_*9244delinsTG | |
ENST00000369878.8:c.*9243_*9244delinsTG | ENSP00000358894.3:n.*9243_*9244delinsTG | |
XR_001747118.1:n.12124_12125delinsTG | ||
XR_001747121.1:n.12088_12089delinsTG | ||
NM_017649.5:c.*9243_*9244delinsTG MANE Select | NP_060119.3:n.*9243_*9244delinsTG | |
NM_199076.3:c.*9243_*9244delinsTG | NP_951058.1:n.*9243_*9244delinsTG |