HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129813838_129813839insGT , CM000671.2:g.129813838_129813839insGT | GRCh38 |
NC_000009.11:g.132576117_132576118insGT , CM000671.1:g.132576117_132576118insGT | GRCh37 |
NC_000009.10:g.131615938_131615939insGT | NCBI36 |
NG_008049.1:g.15325_15326insCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000351698.5:c.*134_*135insCA MANE Select | ENSP00000345719.4:n.*134_*135insCA | |
ENST00000651202.1:c.*401_*402insCA | ENSP00000498222.1:n.*401_*402insCA | |
ENST00000351698.4:c.*134_*135insCA | ENSP00000345719.4:n.*134_*135insCA | |
ENST00000474192.1:n.717_718insCA | ||
NM_000113.2:c.*134_*135insCA | NP_000104.1:n.*134_*135insCA | |
XR_929731.3:n.1328_1329insCA | ||
NM_000113.3:c.*134_*135insCA MANE Select | NP_000104.1:n.*134_*135insCA |