HGVS | Genome Assembly |
---|---|
NC_000013.11:g.50816496_50816499del , CM000675.2:g.50816496_50816499del | GRCh38 |
NC_000013.10:g.51390632_51390635del , CM000675.1:g.51390632_51390635del | GRCh37 |
NC_000013.9:g.50288633_50288636del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651265.1:n.569+6694_569+6697del (DLEU7) | ||
ENST00000651397.1:n.426+26689_426+26692del (DLEU7) | ||
ENST00000400393.3:c.459+26689_459+26692del (DLEU7) | ENSP00000420976.1:n.459+26689_459+26692del | |
NM_198989.2:c.459+26689_459+26692del (DLEU7) | NP_945340.2:n.459+26689_459+26692del | |
NM_198989.3:c.459+26689_459+26692del (DLEU7) | NP_945340.2:n.459+26689_459+26692del | |
NR_046551.1:n.300-2025_300-2022del (DLEU7-AS1) | ||
XM_011534973.1:c.459+26689_459+26692del (DLEU7) | XP_011533275.1:n.459+26689_459+26692del |