HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98187061_98187062insAA , CM000669.2:g.98187061_98187062insAA | GRCh38 |
NC_000007.13:g.97816373_97816374insAA , CM000669.1:g.97816373_97816374insAA | GRCh37 |
NC_000007.12:g.97654309_97654310insAA | NCBI36 |
NG_013375.1:g.85177_85178insAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297293.6:c.998+63_998+64insAA MANE Select | ENSP00000297293.5:n.998+63_998+64insAA | |
ENST00000297293.5:c.998+63_998+64insAA | ENSP00000297293.5:n.998+63_998+64insAA | |
NM_014916.3:c.998+63_998+64insAA | NP_055731.2:n.998+63_998+64insAA | |
XM_011515981.1:c.992+63_992+64insAA | XP_011514283.1:n.992+63_992+64insAA | |
XM_011515981.3:c.992+63_992+64insAA | XP_011514283.1:n.992+63_992+64insAA | |
NM_014916.4:c.998+63_998+64insAA MANE Select | NP_055731.2:n.998+63_998+64insAA |