Linked Data
MyVariant Identifiers:
chr14:g.23891534_23891535insATCATCCACTTGCTGCTCCAGCTTGACTTTGGCCTTAGTCAGGGTGTTGAC (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23422325_23422326insATCATCCACTTGCTGCTCCAGCTTGACTTTGGCCTTAGTCAGGGTGTTGAC , CM000676.2:g.23422325_23422326insATCATCCACTTGCTGCTCCAGCTTGACTTTGGCCTTAGTCAGGGTGTTGAC | GRCh38 |
| NC_000014.8:g.23891534_23891535insATCATCCACTTGCTGCTCCAGCTTGACTTTGGCCTTAGTCAGGGTGTTGAC , CM000676.1:g.23891534_23891535insATCATCCACTTGCTGCTCCAGCTTGACTTTGGCCTTAGTCAGGGTGTTGAC | GRCh37 |
| NC_000014.7:g.22961374_22961375insATCATCCACTTGCTGCTCCAGCTTGACTTTGGCCTTAGTCAGGGTGTTGAC | NCBI36 |
| NG_007884.1:g.18336_18337insGTCAACACCCTGACTAAGGCCAAAGTCAAGCTGGAGCAGCAAGTGGATGAT , LRG_384:g.18336_18337insGTCAACACCCTGACTAAGGCCAAAGTCAAGCTGGAGCAGCAAGTGGATGAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.3100-1_3100insGTCAACACCCTGACTAAGGCCAAAGTCAAGCTGGAGCAGCAAGTGGATGAT MANE Select | ENSP00000347507.3:n.3100-1_3100insGTCAACACCCTGACTAAGGCCAAAGTC... | |
| ENST00000355349.3:c.3100-1_3100insGTCAACACCCTGACTAAGGCCAAAGTCAAGCTGGAGCAGCAAGTGGATGAT | ENSP00000347507.3:n.3100-1_3100insGTCAACACCCTGACTAAGGCCAAAGTC... | |
| NM_000257.3:c.3100-1_3100insGTCAACACCCTGACTAAGGCCAAAGTCAAGCTGGAGCAGCAAGTGGATGAT | NP_000248.2:n.3100-1_3100insGTCAACACCCTGACTAAGGCCAAAGTCAAGCTG... | |
| XR_245686.3:n.3206-1_3206insGTCAACACCCTGACTAAGGCCAAAGTCAAGCTGGAGCAGCAAGTGGATGAT | ||
| XM_017021340.1:c.3100-1_3100insGTCAACACCCTGACTAAGGCCAAAGTCAAGCTGGAGCAGCAAGTGGATGAT | XP_016876829.1:n.3100-1_3100insGTCAACACCCTGACTAAGGCCAAAGTCAAG... | |
| NM_000257.4:c.3100-1_3100insGTCAACACCCTGACTAAGGCCAAAGTCAAGCTGGAGCAGCAAGTGGATGAT MANE Select | NP_000248.2:n.3100-1_3100insGTCAACACCCTGACTAAGGCCAAAGTCAAGCTG... |