HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648428_152648429delinsAG , CM000669.2:g.152648428_152648429delinsAG | GRCh38 |
NC_000007.13:g.152345513_152345514delinsAG , CM000669.1:g.152345513_152345514delinsAG | GRCh37 |
NC_000007.12:g.151976446_151976447delinsAG | NCBI36 |
NG_027988.1:g.32737_32738delinsCT | |
NG_027988.2:g.32737_32738delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.*213_*214delinsCT | ENSP00000513758.1:n.*213_*214delinsCT | |
ENST00000359321.2:c.*213_*214delinsCT MANE Select | ENSP00000352271.1:n.*213_*214delinsCT | |
ENST00000359321.1:c.*213_*214delinsCT | ENSP00000352271.1:n.*213_*214delinsCT | |
ENST00000495707.1:n.1078_1079delinsCT | ||
NM_005431.1:c.*213_*214delinsCT | NP_005422.1:n.*213_*214delinsCT | |
NM_005431.2:c.*213_*214delinsCT MANE Select | NP_005422.1:n.*213_*214delinsCT |