HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86739620_86739624delinsGTTTT , CM000670.2:g.86739620_86739624delinsGTTTT | GRCh38 |
NC_000008.10:g.87751848_87751852delinsGTTTT , CM000670.1:g.87751848_87751852delinsGTTTT | GRCh37 |
NC_000008.9:g.87820964_87820968delinsGTTTT | NCBI36 |
NG_016980.1:g.9052_9056delinsAAAAC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000320005.6:c.211+31_211+35delinsAAAAC MANE Select | ENSP00000316605.5:n.211+31_211+35delinsAA... | |
ENST00000681746.1:c.211+31_211+35delinsAAAAC | ENSP00000505959.1:n.211+31_211+35delinsAA... | |
ENST00000320005.5:c.211+31_211+35delinsAAAAC | ENSP00000316605.5:n.211+31_211+35delinsAA... | |
ENST00000519777.1:n.193+31_193+35delinsAAAAC | ||
NM_019098.4:c.211+31_211+35delinsAAAAC | NP_061971.3:n.211+31_211+35delinsAAAAC | |
NM_019098.5:c.211+31_211+35delinsAAAAC MANE Select | NP_061971.3:n.211+31_211+35delinsAAAAC |