HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8731833del , CM000685.2:g.8731833del | GRCh38 |
NC_000023.10:g.8699874del , CM000685.1:g.8699874del | GRCh37 |
NC_000023.9:g.8659874del | NCBI36 |
NG_007088.1:g.5355del | |
NG_007088.2:g.5355del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262648.8:c.205del MANE Select | ENSP00000262648.3:p.Gln69ArgfsTer28 | |
ENST00000262648.7:c.205del | ENSP00000262648.3:p.Gln69ArgfsTer28 | |
ENST00000619786.1:c.202del | ENSP00000478734.1:p.Gln68ArgfsTer28 | |
NM_000216.2:c.205del | NP_000207.2:p.Gln69ArgfsTer28 | |
XM_005274501.3:c.205del | XP_005274558.1:p.Gln69ArgfsTer28 | |
NM_000216.3:c.205del | NP_000207.2:p.Gln69ArgfsTer28 | |
XM_005274501.4:c.205del | XP_005274558.1:p.Gln69ArgfsTer28 | |
NM_000216.4:c.205del MANE Select | NP_000207.2:p.Gln69ArgfsTer28 |