HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071712_111071713insTCCCTG , CM000667.2:g.111071712_111071713insTCCCTG | GRCh38 |
NC_000005.9:g.110407410_110407411insTCCCTG , CM000667.1:g.110407410_110407411insTCCCTG | GRCh37 |
NC_000005.8:g.110435309_110435310insTCCCTG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.-178-1_-178insTCCCTG MANE Select | ENSP00000339804.3:n.-178-1_-178insTCCCTG | |
ENST00000344895.3:c.-179_-178insTCCCTG | ENSP00000339804.3:n.-179_-178insTCCCTG | |
ENST00000420978.6:c.34+195_34+196insTCCCTG | ENSP00000399099.2:n.34+195_34+196insTCCCTG | |
NM_033035.4:c.-179_-178insTCCCTG | NP_149024.1:n.-179_-178insTCCCTG | |
NR_045089.1:n.1438+195_1438+196insTCCCTG | ||
NM_033035.5:c.-178-1_-178insTCCCTG MANE Select | NP_149024.1:n.-178-1_-178insTCCCTG | |
NR_045089.2:n.1456+195_1456+196insTCCCTG |