HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149569913_149569917del , CM000664.2:g.149569913_149569917del | GRCh38 |
NC_000002.11:g.150426427_150426431del , CM000664.1:g.150426427_150426431del | GRCh37 |
NC_000002.10:g.150134673_150134677del | NCBI36 |
NG_009189.1:g.22900_22904del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.*57_*61del MANE Select | ENSP00000301920.5:n.*57_*61del | |
ENST00000303319.9:c.*57_*61del | ENSP00000301920.5:n.*57_*61del | |
ENST00000422782.2:c.*57_*61del | ENSP00000408331.2:n.*57_*61del | |
ENST00000428879.5:c.*57_*61del | ENSP00000389060.1:n.*57_*61del | |
NM_015702.2:c.*57_*61del | NP_056517.1:n.*57_*61del | |
NM_015702.3:c.*57_*61del MANE Select | NP_056517.1:n.*57_*61del |