HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149569702_149569705delinsAGAG , CM000664.2:g.149569702_149569705delinsAGAG | GRCh38 |
NC_000002.11:g.150426216_150426219delinsAGAG , CM000664.1:g.150426216_150426219delinsAGAG | GRCh37 |
NC_000002.10:g.150134462_150134465delinsAGAG | NCBI36 |
NG_009189.1:g.23112_23115delinsCTCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.*269_*272delinsCTCT MANE Select | ENSP00000301920.5:n.*269_*272delinsCTCT | |
ENST00000303319.9:c.*269_*272delinsCTCT | ENSP00000301920.5:n.*269_*272delinsCTCT | |
ENST00000422782.2:c.*269_*272delinsCTCT | ENSP00000408331.2:n.*269_*272delinsCTCT | |
ENST00000428879.5:c.*269_*272delinsCTCT | ENSP00000389060.1:n.*269_*272delinsCTCT | |
NM_015702.2:c.*269_*272delinsCTCT | NP_056517.1:n.*269_*272delinsCTCT | |
NM_015702.3:c.*269_*272delinsCTCT MANE Select | NP_056517.1:n.*269_*272delinsCTCT |