HGVS | Genome Assembly |
---|---|
NC_000007.14:g.17339711_17339714delinsAAGT , CM000669.2:g.17339711_17339714delinsAAGT | GRCh38 |
NC_000007.13:g.17379335_17379338delinsAAGT , CM000669.1:g.17379335_17379338delinsAAGT | GRCh37 |
NC_000007.12:g.17345860_17345863delinsAAGT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242057.9:c.1886_1889delinsAAGT MANE Select | ENSP00000242057.4:p.Gln629= | |
ENST00000637807.1:c.1856_1859delinsAAGT | ENSP00000490530.1:p.Gln619= | |
ENST00000642825.1:c.1841_1844delinsAAGT | ENSP00000495987.1:p.Gln614= | |
ENST00000242057.8:c.1886_1889delinsAAGT | ENSP00000242057.4:p.Gln629= | |
ENST00000463496.1:c.1886_1889delinsAAGT | ENSP00000436466.1:p.Gln629= | |
NM_001621.4:c.1886_1889delinsAAGT | NP_001612.1:p.Gln629= | |
NM_001621.5:c.1886_1889delinsAAGT MANE Select | NP_001612.1:p.Gln629= |