HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648424_152648429delinsAAAAAG , CM000669.2:g.152648424_152648429delinsAAAAAG | GRCh38 |
NC_000007.13:g.152345509_152345514delinsAAAAAG , CM000669.1:g.152345509_152345514delinsAAAAAG | GRCh37 |
NC_000007.12:g.151976442_151976447delinsAAAAAG | NCBI36 |
NG_027988.1:g.32737_32742delinsCTTTTT | |
NG_027988.2:g.32737_32742delinsCTTTTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.*213_*218delinsCTTTTT | ENSP00000513758.1:n.*213_*218delinsCTTTTT | |
ENST00000359321.2:c.*213_*218delinsCTTTTT MANE Select | ENSP00000352271.1:n.*213_*218delinsCTTTTT | |
ENST00000359321.1:c.*213_*218delinsCTTTTT | ENSP00000352271.1:n.*213_*218delinsCTTTTT | |
ENST00000495707.1:n.1078_1083delinsCTTTTT | ||
NM_005431.1:c.*213_*218delinsCTTTTT | NP_005422.1:n.*213_*218delinsCTTTTT | |
NM_005431.2:c.*213_*218delinsCTTTTT MANE Select | NP_005422.1:n.*213_*218delinsCTTTTT |