Linked Data
dbSNP Id:
rs762589363
ExAC:
4:187209640 A / ATTG
gnomAD v2:
4-187209640-A-ATTG
MyVariant Identifiers:
chr4:g.187209640_187209641insTTG (hg19)
chr4:g.186288486_186288487insTTG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186288486_186288487insTTG , CM000666.2:g.186288486_186288487insTTG | GRCh38 |
| NC_000004.11:g.187209640_187209641insTTG , CM000666.1:g.187209640_187209641insTTG | GRCh37 |
| NC_000004.10:g.187446634_187446635insTTG | NCBI36 |
| NG_008051.1:g.27523_27524insTTG , LRG_583:g.27523_27524insTTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403665.7:c.1750_1751insTTG (F11) MANE Select | ENSP00000384957.2:p.Asn584delinsIleAsp | |
| ENST00000264691.4:c.350_351insTTG (F11) | ||
| ENST00000264692.8:c.1588_1589insTTG (F11) | ENSP00000264692.5:p.Asn530delinsIleAsp | |
| ENST00000403665.6:c.1750_1751insTTG (F11) | ENSP00000384957.2:p.Asn584delinsIleAsp | |
| ENST00000503841.1:n.269_270insTTG (F11) | ||
| NM_000128.3:c.1750_1751insTTG , LRG_583t1:c.1750_1751insTTG (F11) | NP_000119.1:p.Asn584delinsIleAsp | |
| NR_033900.1:n.1007_1008insCAA (F11-AS1) | ||
| XM_005262821.2:c.1753_1754insTTG (F11) | XP_005262878.1:p.Asn585delinsIleAsp | |
| XM_005262822.2:c.1657_1658insTTG (F11) | XP_005262879.1:p.Asn553delinsIleAsp | |
| XM_005262823.2:c.1483_1484insTTG (F11) | XP_005262880.1:p.Asn495delinsIleAsp | |
| XM_006714137.1:c.1705_1706insTTG (F11) | XP_006714200.1:p.Asn569delinsIleAsp | |
| XM_005262821.4:c.1753_1754insTTG (F11) | XP_005262878.1:p.Asn585delinsIleAsp | |
| XM_005262822.4:c.1657_1658insTTG (F11) | XP_005262879.1:p.Asn553delinsIleAsp | |
| XM_005262823.4:c.1483_1484insTTG (F11) | XP_005262880.1:p.Asn495delinsIleAsp | |
| XM_006714137.3:c.1705_1706insTTG (F11) | XP_006714200.1:p.Asn569delinsIleAsp | |
| NM_000128.4:c.1750_1751insTTG (F11) MANE Select | NP_000119.1:p.Asn584delinsIleAsp |