HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071802_111071803insT , CM000667.2:g.111071802_111071803insT | GRCh38 |
NC_000005.9:g.110407500_110407501insT , CM000667.1:g.110407500_110407501insT | GRCh37 |
NC_000005.8:g.110435399_110435400insT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.-89_-88insT MANE Select | ENSP00000339804.3:n.-89_-88insT | |
ENST00000344895.3:c.-89_-88insT | ENSP00000339804.3:n.-89_-88insT | |
ENST00000420978.6:c.35-123_35-122insT | ENSP00000399099.2:n.35-123_35-122insT | |
NM_033035.4:c.-89_-88insT | NP_149024.1:n.-89_-88insT | |
NR_045089.1:n.1439-123_1439-122insT | ||
NM_033035.5:c.-89_-88insT MANE Select | NP_149024.1:n.-89_-88insT | |
NR_045089.2:n.1457-123_1457-122insT |