HGVS | Genome Assembly |
---|---|
NC_000023.11:g.151181416_151181424del , CM000685.2:g.151181416_151181424del | GRCh38 |
NC_000023.10:g.150349888_150349896del , CM000685.1:g.150349888_150349896del | GRCh37 |
NC_000023.9:g.150100546_150100554del | NCBI36 |
NG_016405.1:g.9833_9841del | |
NG_016405.2:g.9833_9841del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218316.4:c.1833_1841del MANE Select | ENSP00000218316.3:p.Asp611_Asp613del | |
ENST00000218316.3:c.1833_1841del | ENSP00000218316.3:p.Asp611_Asp613del | |
ENST00000617907.1:c.1827_1835del | ENSP00000484496.1:p.Asp609_Asp611del | |
NM_004224.3:c.1833_1841del MANE Select | NP_004215.2:p.Asp611_Asp613del | |
XM_011531216.1:c.1092_1100del | XP_011529518.1:p.Asp364_Asp366del | |
XM_011531216.2:c.1092_1100del | XP_011529518.1:p.Asp364_Asp366del |