HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70177147_70177152delinsCTTGAA , CM000679.2:g.70177147_70177152delinsCTTGAA | GRCh38 |
NC_000017.10:g.68173288_68173293delinsCTTGAA , CM000679.1:g.68173288_68173293delinsCTTGAA | GRCh37 |
NC_000017.9:g.65684883_65684888delinsCTTGAA | NCBI36 |
NG_008798.1:g.12613_12618delinsCTTGAA , LRG_328:g.12613_12618delinsCTTGAA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000243457.4:c.*824_*829delinsCTTGAA MANE Select | ENSP00000243457.2:n.*824_*829delinsCTTGAA | |
ENST00000243457.3:c.*824_*829delinsCTTGAA | ENSP00000243457.2:n.*824_*829delinsCTTGAA | |
NM_000891.2:c.*824_*829delinsCTTGAA , LRG_328t1:c.*824_*829delinsCTTGAA | NP_000882.1:n.*824_*829delinsCTTGAA | |
XM_011524779.1:c.*824_*829delinsCTTGAA | XP_011523081.1:n.*824_*829delinsCTTGAA | |
NM_000891.3:c.*824_*829delinsCTTGAA MANE Select | NP_000882.1:n.*824_*829delinsCTTGAA |