HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159316140_159316141insTC , CM000667.2:g.159316140_159316141insTC | GRCh38 |
NC_000005.9:g.158743148_158743149insTC , CM000667.1:g.158743148_158743149insTC | GRCh37 |
NC_000005.8:g.158675726_158675727insTC | NCBI36 |
NG_009618.1:g.19333_19334insGA , LRG_71:g.19333_19334insGA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*1-41_*1-40insGA | ENSP00000512849.1:n.*1-41_*1-40insGA | |
ENST00000696751.1:c.*483-41_*483-40insGA | ENSP00000512850.1:n.*483-41_*483-40insGA | |
ENST00000231228.3:c.*1-41_*1-40insGA MANE Select | ENSP00000231228.2:n.*1-41_*1-40insGA | |
ENST00000231228.2:c.*1-41_*1-40insGA | ENSP00000231228.2:n.*1-41_*1-40insGA | |
NM_002187.2:c.*1-41_*1-40insGA , LRG_71t1:c.*1-41_*1-40insGA | NP_002178.2:n.*1-41_*1-40insGA | |
NM_002187.3:c.*1-41_*1-40insGA MANE Select | NP_002178.2:n.*1-41_*1-40insGA |