HGVS | Genome Assembly |
---|---|
NC_000023.11:g.101348703_101348704insT , CM000685.2:g.101348703_101348704insT | GRCh38 |
NC_000023.10:g.100603691_100603692insT , CM000685.1:g.100603691_100603692insT | GRCh37 |
NC_000023.9:g.100490347_100490348insT | NCBI36 |
NG_009616.1:g.42521_42522insA , LRG_128:g.42521_42522insA | |
NG_011734.1:g.5266_5267insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372902.4:c.-40_-39insA MANE Select | ENSP00000361993.3:n.-40_-39insA | |
ENST00000644112.2:c.-40_-39insA | ENSP00000494385.1:n.-40_-39insA | |
ENST00000372902.3:c.-40_-39insA | ENSP00000361993.3:n.-40_-39insA | |
ENST00000480575.1:n.46_47insA | ||
NM_001145951.1:c.-40_-39insA | NP_001139423.1:n.-40_-39insA | |
NM_004085.3:c.-40_-39insA | NP_004076.1:n.-40_-39insA | |
NM_004085.4:c.-40_-39insA MANE Select | NP_004076.1:n.-40_-39insA | |
NM_001145951.2:c.-40_-39insA | NP_001139423.1:n.-40_-39insA |