HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29071040_29071041delinsTG , CM000664.2:g.29071040_29071041delinsTG | GRCh38 |
NC_000002.11:g.29293906_29293907delinsTG , CM000664.1:g.29293906_29293907delinsTG | GRCh37 |
NC_000002.10:g.29147410_29147411delinsTG | NCBI36 |
NG_021427.1:g.8221_8222delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.3221_3222delinsCA MANE Select | ENSP00000332809.4:p.Pro1074= | |
ENST00000331664.5:c.3221_3222delinsCA | ENSP00000332809.4:p.Pro1074= | |
NM_001029883.2:c.3221_3222delinsCA | NP_001025054.1:p.Pro1074= | |
XM_011532826.1:c.3221_3222delinsCA | XP_011531128.1:p.Pro1074= | |
XR_939901.1:n.185+1873_185+1874delinsTG | ||
XR_939902.1:n.173+1885_173+1886delinsTG | ||
NM_001029883.3:c.3221_3222delinsCA MANE Select | NP_001025054.1:p.Pro1074= |