Linked Data
dbSNP Id:
rs1289108033
MyVariant Identifiers:
chr4:g.187208756_187208757insTG (hg19)
chr4:g.186287602_186287603insTG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186287603_186287604insGT , CM000666.2:g.186287603_186287604insGT | GRCh38 |
| NC_000004.11:g.187208757_187208758insGT , CM000666.1:g.187208757_187208758insGT | GRCh37 |
| NC_000004.10:g.187445751_187445752insGT | NCBI36 |
| NG_008051.1:g.26640_26641insGT , LRG_583:g.26640_26641insGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403665.7:c.1577-81_1577-80insGT (F11) MANE Select | ENSP00000384957.2:n.1577-81_1577-80insGT | |
| ENST00000264691.4:c.177-81_177-80insGT (F11) | ||
| ENST00000264692.8:c.1415-81_1415-80insGT (F11) | ENSP00000264692.5:n.1415-81_1415-80insGT | |
| ENST00000403665.6:c.1577-81_1577-80insGT (F11) | ENSP00000384957.2:n.1577-81_1577-80insGT | |
| ENST00000503841.1:n.15_16insGT (F11) | ||
| NM_000128.3:c.1577-81_1577-80insGT , LRG_583t1:c.1577-81_1577-80insGT (F11) | NP_000119.1:n.1577-81_1577-80insGT | |
| NR_033900.1:n.1066+825_1066+826insCA (F11-AS1) | ||
| XM_005262821.2:c.1580-81_1580-80insGT (F11) | XP_005262878.1:n.1580-81_1580-80insGT | |
| XM_005262822.2:c.1484-81_1484-80insGT (F11) | XP_005262879.1:n.1484-81_1484-80insGT | |
| XM_005262823.2:c.1310-81_1310-80insGT (F11) | XP_005262880.1:n.1310-81_1310-80insGT | |
| XM_006714137.1:c.1532-81_1532-80insGT (F11) | XP_006714200.1:n.1532-81_1532-80insGT | |
| XR_938706.1:n.1985-81_1985-80insGT (F11) | ||
| XR_938707.1:n.1889-81_1889-80insGT (F11) | ||
| XM_005262821.4:c.1580-81_1580-80insGT (F11) | XP_005262878.1:n.1580-81_1580-80insGT | |
| XM_005262822.4:c.1484-81_1484-80insGT (F11) | XP_005262879.1:n.1484-81_1484-80insGT | |
| XM_005262823.4:c.1310-81_1310-80insGT (F11) | XP_005262880.1:n.1310-81_1310-80insGT | |
| XM_006714137.3:c.1532-81_1532-80insGT (F11) | XP_006714200.1:n.1532-81_1532-80insGT | |
| NM_000128.4:c.1577-81_1577-80insGT (F11) MANE Select | NP_000119.1:n.1577-81_1577-80insGT |