HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116172545_116172546insA , CM000685.2:g.116172545_116172546insA | GRCh38 |
NC_000023.10:g.115303798_115303799insA , CM000685.1:g.115303798_115303799insA | GRCh37 |
NC_000023.9:g.115217826_115217827insA | NCBI36 |
NG_016326.1:g.6841_6842insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.265_266insA MANE Select | ENSP00000360973.4:p.Ala89AspfsTer2 | |
ENST00000680409.1:n.733_734insA | ||
ENST00000681852.1:c.265_266insA | ENSP00000505750.1:p.Ala89AspfsTer2 | |
ENST00000371906.4:c.265_266insA | ENSP00000360973.4:p.Ala89AspfsTer2 | |
NM_000686.4:c.265_266insA | NP_000677.2:p.Ala89AspfsTer2 | |
XM_011537533.1:c.265_266insA | XP_011535835.1:p.Ala89AspfsTer2 | |
NM_000686.5:c.265_266insA MANE Select | NP_000677.2:p.Ala89AspfsTer2 | |
NM_001385624.1:c.265_266insA | NP_001372553.1:p.Ala89AspfsTer2 |