HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6031723_6031724insTGGGT , CM000674.2:g.6031723_6031724insTGGGT | GRCh38 |
NC_000012.11:g.6140889_6140890insTGGGT , CM000674.1:g.6140889_6140890insTGGGT | GRCh37 |
NC_000012.10:g.6011150_6011151insTGGGT | NCBI36 |
NG_009072.1:g.97949_97950insCCAAC | |
NG_009072.2:g.97949_97950insCCAAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261405.10:c.2686-144_2686-143insCCAAC MANE Select | ENSP00000261405.5:n.2686-144_2686-143insCCAAC | |
ENST00000261405.9:c.2686-144_2686-143insCCAAC | ENSP00000261405.5:n.2686-144_2686-143insCCAAC | |
ENST00000538635.5:n.421-37788_421-37787insCCAAC | ||
NM_000552.3:c.2686-144_2686-143insCCAAC | NP_000543.2:n.2686-144_2686-143insCCAAC | |
NM_000552.4:c.2686-144_2686-143insCCAAC | NP_000543.2:n.2686-144_2686-143insCCAAC | |
NM_000552.5:c.2686-144_2686-143insCCAAC MANE Select | NP_000543.3:n.2686-144_2686-143insCCAAC |