HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135856562_135856567delinsCTTTAT , CM000664.2:g.135856562_135856567delinsCTTTAT | GRCh38 |
NC_000002.11:g.136614132_136614137delinsCTTTAT , CM000664.1:g.136614132_136614137delinsCTTTAT | GRCh37 |
NC_000002.10:g.136330602_136330607delinsCTTTAT | NCBI36 |
NG_008104.2:g.3603_3608delinsATAAAG , LRG_338:g.3603_3608delinsATAAAG | |
NG_008958.1:g.24875_24880delinsATAAAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264156.3:c.1626+161_1626+166delinsATAAAG MANE Select | ENSP00000264156.2:n.1626+161_1626+166delinsATAAAG | |
ENST00000264156.2:c.1626+161_1626+166delinsATAAAG | ENSP00000264156.2:n.1626+161_1626+166delinsATAAAG | |
ENST00000492091.1:n.182-5004_182-4999delinsATAAAG | ||
NM_005915.5:c.1626+161_1626+166delinsATAAAG | NP_005906.2:n.1626+161_1626+166delinsATAAAG | |
NM_005915.6:c.1626+161_1626+166delinsATAAAG MANE Select | NP_005906.2:n.1626+161_1626+166delinsATAAAG |