HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38146061_38146062insT , CM000670.2:g.38146061_38146062insT | GRCh38 |
NC_000008.10:g.38003579_38003580insT , CM000670.1:g.38003579_38003580insT | GRCh37 |
NC_000008.9:g.38122736_38122737insT | NCBI36 |
NG_011827.1:g.10021_10022insA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000276449.9:c.551_552insA MANE Select | ENSP00000276449.3:p.Phe184LeufsTer28 | |
ENST00000276449.8:c.551_552insA | ENSP00000276449.3:p.Phe184LeufsTer28 | |
ENST00000520114.1:n.1038_1039insA | ||
ENST00000522050.1:c.487_488insA | ||
NM_000349.2:c.551_552insA | NP_000340.2:p.Phe184LeufsTer28 | |
XM_006716392.1:c.551_552insA | XP_006716455.1:p.Phe184LeufsTer28 | |
NM_000349.3:c.551_552insA MANE Select | NP_000340.2:p.Phe184LeufsTer28 |