HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6023896_6023897insTTG , CM000674.2:g.6023896_6023897insTTG | GRCh38 |
NC_000012.11:g.6133062_6133063insTTG , CM000674.1:g.6133062_6133063insTTG | GRCh37 |
NC_000012.10:g.6003323_6003324insTTG | NCBI36 |
NG_009072.1:g.105774_105775insCAA | |
NG_009072.2:g.105774_105775insCAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261405.10:c.3223-110_3223-109insCAA MANE Select | ENSP00000261405.5:n.3223-110_3223-109insCAA | |
ENST00000261405.9:c.3223-110_3223-109insCAA | ENSP00000261405.5:n.3223-110_3223-109insCAA | |
ENST00000538635.5:n.421-29963_421-29962insCAA | ||
NM_000552.3:c.3223-110_3223-109insCAA | NP_000543.2:n.3223-110_3223-109insCAA | |
NM_000552.4:c.3223-110_3223-109insCAA | NP_000543.2:n.3223-110_3223-109insCAA | |
NM_000552.5:c.3223-110_3223-109insCAA MANE Select | NP_000543.3:n.3223-110_3223-109insCAA |