HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648425_152648429delinsAAAAG , CM000669.2:g.152648425_152648429delinsAAAAG | GRCh38 |
NC_000007.13:g.152345510_152345514delinsAAAAG , CM000669.1:g.152345510_152345514delinsAAAAG | GRCh37 |
NC_000007.12:g.151976443_151976447delinsAAAAG | NCBI36 |
NG_027988.1:g.32737_32741delinsCTTTT | |
NG_027988.2:g.32737_32741delinsCTTTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.*213_*217delinsCTTTT | ENSP00000513758.1:n.*213_*217delinsCTTTT | |
ENST00000359321.2:c.*213_*217delinsCTTTT MANE Select | ENSP00000352271.1:n.*213_*217delinsCTTTT | |
ENST00000359321.1:c.*213_*217delinsCTTTT | ENSP00000352271.1:n.*213_*217delinsCTTTT | |
ENST00000495707.1:n.1078_1082delinsCTTTT | ||
NM_005431.1:c.*213_*217delinsCTTTT | NP_005422.1:n.*213_*217delinsCTTTT | |
NM_005431.2:c.*213_*217delinsCTTTT MANE Select | NP_005422.1:n.*213_*217delinsCTTTT |