HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70176048_70176050del , CM000679.2:g.70176048_70176050del | GRCh38 |
NC_000017.10:g.68172189_68172191del , CM000679.1:g.68172189_68172191del | GRCh37 |
NC_000017.9:g.65683784_65683786del | NCBI36 |
NG_008798.1:g.11514_11516del , LRG_328:g.11514_11516del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243457.4:c.1009_1011del MANE Select | ENSP00000243457.2:p.Tyr337del | |
ENST00000243457.3:c.1009_1011del | ENSP00000243457.2:p.Tyr337del | |
ENST00000535240.1:c.1009_1011del | ENSP00000441848.1:p.Tyr337del | |
NM_000891.2:c.1009_1011del , LRG_328t1:c.1009_1011del | NP_000882.1:p.Tyr337del | |
XM_011524779.1:c.1009_1011del | XP_011523081.1:p.Tyr337del | |
NM_000891.3:c.1009_1011del MANE Select | NP_000882.1:p.Tyr337del |