HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648560_152648561delinsTG , CM000669.2:g.152648560_152648561delinsTG | GRCh38 |
NC_000007.13:g.152345645_152345646delinsTG , CM000669.1:g.152345645_152345646delinsTG | GRCh37 |
NC_000007.12:g.151976578_151976579delinsTG | NCBI36 |
NG_027988.1:g.32605_32606delinsCA | |
NG_027988.2:g.32605_32606delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.*81_*82delinsCA | ENSP00000513758.1:n.*81_*82delinsCA | |
ENST00000359321.2:c.*81_*82delinsCA MANE Select | ENSP00000352271.1:n.*81_*82delinsCA | |
ENST00000359321.1:c.*81_*82delinsCA | ENSP00000352271.1:n.*81_*82delinsCA | |
ENST00000495707.1:n.946_947delinsCA | ||
NM_005431.1:c.*81_*82delinsCA | NP_005422.1:n.*81_*82delinsCA | |
NM_005431.2:c.*81_*82delinsCA MANE Select | NP_005422.1:n.*81_*82delinsCA |