HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88007720_88007721insCCGG , CM000666.2:g.88007720_88007721insCCGG | GRCh38 |
NC_000004.11:g.88928872_88928873insCCGG , CM000666.1:g.88928872_88928873insCCGG | GRCh37 |
NC_000004.10:g.89147896_89147897insCCGG | NCBI36 |
NG_008604.1:g.5053_5054insCCGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.-14_-13insCCGG MANE Select | ENSP00000237596.2:n.-14_-13insCCGG | |
ENST00000237596.6:c.-14_-13insCCGG | ENSP00000237596.2:n.-14_-13insCCGG | |
NM_000297.3:c.-14_-13insCCGG | NP_000288.1:n.-14_-13insCCGG | |
XM_011532028.1:c.-14_-13insCCGG | XP_011530330.1:n.-14_-13insCCGG | |
XR_244632.2:n.82_83insCCGG | ||
NR_156488.1:n.74_75insCCGG | ||
XM_011532028.2:c.-14_-13insCCGG | XP_011530330.1:n.-14_-13insCCGG | |
NM_000297.4:c.-14_-13insCCGG MANE Select | NP_000288.1:n.-14_-13insCCGG | |
NR_156488.2:n.86_87insCCGG |