HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29070645_29070646insT , CM000664.2:g.29070645_29070646insT | GRCh38 |
NC_000002.11:g.29293511_29293512insT , CM000664.1:g.29293511_29293512insT | GRCh37 |
NC_000002.10:g.29147015_29147016insT | NCBI36 |
NG_021427.1:g.8616_8617insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.3616_3617insA MANE Select | ENSP00000332809.4:p.Pro1206HisfsTer11 | |
ENST00000331664.5:c.3616_3617insA | ENSP00000332809.4:p.Pro1206HisfsTer11 | |
NM_001029883.2:c.3616_3617insA | NP_001025054.1:p.Pro1206HisfsTer11 | |
XM_011532826.1:c.3616_3617insA | XP_011531128.1:p.Pro1206HisfsTer11 | |
XR_939901.1:n.185+1478_185+1479insT | ||
XR_939902.1:n.173+1490_173+1491insT | ||
NM_001029883.3:c.3616_3617insA MANE Select | NP_001025054.1:p.Pro1206HisfsTer11 |