HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8075567_8075568delinsCT , CM000679.2:g.8075567_8075568delinsCT | GRCh38 |
NC_000017.10:g.7978885_7978886delinsCT , CM000679.1:g.7978885_7978886delinsCT | GRCh37 |
NC_000017.9:g.7919610_7919611delinsCT | NCBI36 |
NG_007099.1:g.17136_17137delinsAG | |
NG_007099.2:g.17149_17150delinsAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647874.1:c.1654+27_1654+28delinsAG MANE Select | ENSP00000497784.1:n.1654+27_1654+28delinsAG | |
ENST00000649809.1:c.718+27_718+28delinsAG | ENSP00000496845.1:n.718+27_718+28delinsAG | |
ENST00000319144.4:c.1654+27_1654+28delinsAG | ENSP00000315167.4:n.1654+27_1654+28delinsAG | |
ENST00000577351.5:n.479+607_479+608delinsAG | ||
NM_001139.2:c.1654+27_1654+28delinsAG | NP_001130.1:n.1654+27_1654+28delinsAG | |
NM_001139.3:c.1654+27_1654+28delinsAG MANE Select | NP_001130.1:n.1654+27_1654+28delinsAG |