HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1611804_1611806dup , CM000668.2:g.1611804_1611806dup | GRCh38 |
NC_000006.11:g.1612039_1612041dup , CM000668.1:g.1612039_1612041dup | GRCh37 |
NC_000006.10:g.1557038_1557040dup | NCBI36 |
NG_009368.1:g.6359_6361dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645831.2:c.1359_1361dup MANE Select | ENSP00000493906.1:p.Gly454_Gly455insGly | |
ENST00000380874.3:c.1359_1361dup | ENSP00000370256.2:p.Gly454_Gly455insGly | |
NM_001453.2:c.1359_1361dup | NP_001444.2:p.Gly454_Gly455insGly | |
NM_001453.3:c.1359_1361dup MANE Select | NP_001444.2:p.Gly454_Gly455insGly |