HGVS | Genome Assembly |
---|---|
NC_000006.12:g.39048868_39048869delinsCT , CM000668.2:g.39048868_39048869delinsCT | GRCh38 |
NC_000006.11:g.39016644_39016645delinsCT , CM000668.1:g.39016644_39016645delinsCT | GRCh37 |
NC_000006.10:g.39124622_39124623delinsCT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373256.5:c.28_29delinsCT MANE Select | ENSP00000362353.4:p.Leu10= | |
ENST00000373256.4:c.28_29delinsCT | ENSP00000362353.4:p.Leu10= | |
NM_002062.3:c.28_29delinsCT | NP_002053.3:p.Leu10= | |
XR_926153.1:n.88_89delinsCT | ||
XR_926154.1:n.88_89delinsCT | ||
XR_926155.1:n.88_89delinsCT | ||
NM_002062.4:c.28_29delinsCT | NP_002053.3:p.Leu10= | |
NR_136562.1:n.88_89delinsCT | ||
NR_136563.1:n.88_89delinsCT | ||
NM_002062.5:c.28_29delinsCT MANE Select | NP_002053.3:p.Leu10= | |
NR_136562.2:n.88_89delinsCT | ||
NR_136563.2:n.88_89delinsCT |