HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31498179_31498184delinsGGAGCC , CM000680.2:g.31498179_31498184delinsGGAGCC | GRCh38 |
NC_000018.9:g.29078142_29078147delinsGGAGCC , CM000680.1:g.29078142_29078147delinsGGAGCC | GRCh37 |
NC_000018.8:g.27332140_27332145delinsGGAGCC | NCBI36 |
NG_007072.3:g.4938_4943delinsGGAGCC , LRG_397:g.4938_4943delinsGGAGCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261590.13:c.-73_-68delinsGGAGCC MANE Select | ENSP00000261590.8:n.-73_-68delinsGGAGCC | |
ENST00000261590.12:c.-73_-68delinsGGAGCC | ENSP00000261590.8:n.-73_-68delinsGGAGCC | |
NM_001943.3:c.-73_-68delinsGGAGCC , LRG_397t1:c.-73_-68delinsGGAGCC | NP_001934.2:n.-73_-68delinsGGAGCC | |
NM_001943.4:c.-73_-68delinsGGAGCC | NP_001934.2:n.-73_-68delinsGGAGCC | |
NM_001943.5:c.-73_-68delinsGGAGCC MANE Select | NP_001934.2:n.-73_-68delinsGGAGCC |