Linked Data
gnomAD v2:
12-21699425-T-TAAGATTTCAATTC
MyVariant Identifiers:
chr12:g.21699425_21699426insAAGATTTCAATTC (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21546491_21546492insAAGATTTCAATTC , CM000674.2:g.21546491_21546492insAAGATTTCAATTC | GRCh38 |
| NC_000012.11:g.21699425_21699426insAAGATTTCAATTC , CM000674.1:g.21699425_21699426insAAGATTTCAATTC | GRCh37 |
| NC_000012.10:g.21590692_21590693insAAGATTTCAATTC | NCBI36 |
| NG_016167.1:g.63356_63357insGAATTGAAATCTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261195.3:c.1423-22_1423-21insGAATTGAAATCTT MANE Select | ENSP00000261195.2:n.1423-22_1423-21insGAATTGAAATCTT | |
| ENST00000647960.1:c.*1425-22_*1425-21insGAATTGAAATCTT | ENSP00000497202.1:n.*1425-22_*1425-21insGAATTGAAATCTT | |
| ENST00000261195.2:c.1423-22_1423-21insGAATTGAAATCTT | ENSP00000261195.2:n.1423-22_1423-21insGAATTGAAATCTT | |
| NM_021957.3:c.1423-22_1423-21insGAATTGAAATCTT | NP_068776.2:n.1423-22_1423-21insGAATTGAAATCTT | |
| XM_005253352.1:c.1423-22_1423-21insGAATTGAAATCTT | XP_005253409.1:n.1423-22_1423-21insGAATTGAAATCTT | |
| XM_005253354.2:c.1204-22_1204-21insGAATTGAAATCTT | XP_005253411.1:n.1204-22_1204-21insGAATTGAAATCTT | |
| XM_006719062.2:c.1423-22_1423-21insGAATTGAAATCTT | XP_006719125.1:n.1423-22_1423-21insGAATTGAAATCTT | |
| XM_006719063.2:c.1192-22_1192-21insGAATTGAAATCTT | XP_006719126.1:n.1192-22_1192-21insGAATTGAAATCTT | |
| NM_021957.4:c.1423-22_1423-21insGAATTGAAATCTT MANE Select | NP_068776.2:n.1423-22_1423-21insGAATTGAAATCTT | |
| XM_006719063.3:c.1192-22_1192-21insGAATTGAAATCTT | XP_006719126.1:n.1192-22_1192-21insGAATTGAAATCTT | |
| XM_024448960.1:c.1423-22_1423-21insGAATTGAAATCTT | XP_024304728.1:n.1423-22_1423-21insGAATTGAAATCTT |