HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315918_159315923del , CM000667.2:g.159315918_159315923del | GRCh38 |
NC_000005.9:g.158742926_158742931del , CM000667.1:g.158742926_158742931del | GRCh37 |
NC_000005.8:g.158675504_158675509del | NCBI36 |
NG_009618.1:g.19551_19556del , LRG_71:g.19551_19556del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*178_*183del | ENSP00000512849.1:n.*178_*183del | |
ENST00000696751.1:c.*660_*665del | ENSP00000512850.1:n.*660_*665del | |
ENST00000231228.3:c.*178_*183del MANE Select | ENSP00000231228.2:n.*178_*183del | |
ENST00000231228.2:c.*178_*183del | ENSP00000231228.2:n.*178_*183del | |
NM_002187.2:c.*178_*183del , LRG_71t1:c.*178_*183del | NP_002178.2:n.*178_*183del | |
NM_002187.3:c.*178_*183del MANE Select | NP_002178.2:n.*178_*183del |