HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213294_1213296delinsCCA , CM000667.2:g.1213294_1213296delinsCCA | GRCh38 |
NC_000005.9:g.1213409_1213411delinsCCA , CM000667.1:g.1213409_1213411delinsCCA | GRCh37 |
NC_000005.8:g.1266409_1266411delinsCCA | NCBI36 |
NG_008282.1:g.16700_16702delinsCCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.664-169_664-167delinsCCA MANE Select | ENSP00000305302.10:n.664-169_664-167delinsCCA | |
ENST00000304460.10:c.664-169_664-167delinsCCA | ENSP00000305302.10:n.664-169_664-167delinsCCA | |
ENST00000515652.5:c.572-169_572-167delinsCCA | ENSP00000425701.1:n.572-169_572-167delinsCCA | |
NM_001003841.2:c.664-169_664-167delinsCCA | NP_001003841.1:n.664-169_664-167delinsCCA | |
NM_001003841.3:c.664-169_664-167delinsCCA MANE Select | NP_001003841.1:n.664-169_664-167delinsCCA |