HGVS | Genome Assembly |
---|---|
NC_000016.10:g.173457_173458insGG , CM000678.2:g.173457_173458insGG | GRCh38 |
NC_000016.9:g.223456_223457insGG , CM000678.1:g.223456_223457insGG | GRCh37 |
NC_000016.8:g.163456_163457insGG | NCBI36 |
NG_000006.1:g.34320_34321insGG | |
NG_059186.1:g.1807_1808insGG | |
NG_059271.1:g.5611_5612insGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251595.11:c.301-15_301-14insGG MANE Select | ENSP00000251595.6:n.301-15_301-14insGG | |
ENST00000251595.10:c.301-15_301-14insGG | ENSP00000251595.6:n.301-15_301-14insGG | |
ENST00000397806.1:c.205-15_205-14insGG | ENSP00000380908.1:n.205-15_205-14insGG | |
ENST00000482565.1:n.437-15_437-14insGG | ||
ENST00000484216.1:n.397_398insGG | ||
NM_000517.4:c.301-15_301-14insGG | NP_000508.1:n.301-15_301-14insGG | |
NM_000517.6:c.301-15_301-14insGG MANE Select | NP_000508.1:n.301-15_301-14insGG |