HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19117360_19117363delinsAGAG , CM000669.2:g.19117360_19117363delinsAGAG | GRCh38 |
NC_000007.13:g.19156983_19156986delinsAGAG , CM000669.1:g.19156983_19156986delinsAGAG | GRCh37 |
NC_000007.12:g.19123508_19123511delinsAGAG | NCBI36 |
NG_008114.1:g.5310_5313delinsCTCT | |
NG_008114.2:g.5310_5313delinsCTCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.-42_-39delinsCTCT MANE Select | ENSP00000242261.5:n.-42_-39delinsCTCT | |
ENST00000242261.5:c.-42_-39delinsCTCT | ENSP00000242261.5:n.-42_-39delinsCTCT | |
NM_000474.3:c.-42_-39delinsCTCT | NP_000465.1:n.-42_-39delinsCTCT | |
XM_011515496.1:c.-42_-39delinsCTCT | XP_011513798.1:n.-42_-39delinsCTCT | |
NR_149001.1:n.310_313delinsCTCT | ||
NM_000474.4:c.-42_-39delinsCTCT MANE Select | NP_000465.1:n.-42_-39delinsCTCT | |
NR_149001.2:n.274_277delinsCTCT |