HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648423_152648429delinsAAAAAAG , CM000669.2:g.152648423_152648429delinsAAAAAAG | GRCh38 |
NC_000007.13:g.152345508_152345514delinsAAAAAAG , CM000669.1:g.152345508_152345514delinsAAAAAAG | GRCh37 |
NC_000007.12:g.151976441_151976447delinsAAAAAAG | NCBI36 |
NG_027988.1:g.32737_32743delinsCTTTTTT | |
NG_027988.2:g.32737_32743delinsCTTTTTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.*213_*219delinsCTTTTTT | ENSP00000513758.1:n.*213_*219delinsCTTTTTT | |
ENST00000359321.2:c.*213_*219delinsCTTTTTT MANE Select | ENSP00000352271.1:n.*213_*219delinsCTTTTTT | |
ENST00000359321.1:c.*213_*219delinsCTTTTTT | ENSP00000352271.1:n.*213_*219delinsCTTTTTT | |
ENST00000495707.1:n.1078_1084delinsCTTTTTT | ||
NM_005431.1:c.*213_*219delinsCTTTTTT | NP_005422.1:n.*213_*219delinsCTTTTTT | |
NM_005431.2:c.*213_*219delinsCTTTTTT MANE Select | NP_005422.1:n.*213_*219delinsCTTTTTT |