HGVS | Genome Assembly |
---|---|
NC_000011.10:g.66560712_66560713insACACACC , CM000673.2:g.66560712_66560713insACACACC | GRCh38 |
NC_000011.9:g.66328183_66328184insACACACC , CM000673.1:g.66328183_66328184insACACACC | GRCh37 |
NC_000011.8:g.66084759_66084760insACACACC | NCBI36 |
NG_013304.2:g.18793_18794insACACACC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000513398.2:c.1817_1818insACACACC MANE Select | ENSP00000426797.1:p.Tyr606Ter | |
ENST00000502692.5:c.1946_1947insACACACC | ENSP00000422007.1:p.Tyr649Ter | |
ENST00000513398.1:c.1817_1818insACACACC | ENSP00000426797.1:p.Tyr606Ter | |
NM_001104.3:c.1817_1818insACACACC | NP_001095.2:p.Tyr606Ter | |
NM_001258371.2:c.1946_1947insACACACC | NP_001245300.2:p.Tyr649Ter | |
NM_001104.4:c.1817_1818insACACACC MANE Select | NP_001095.2:p.Tyr606Ter | |
NM_001258371.3:c.1946_1947insACACACC | NP_001245300.2:p.Tyr649Ter |