Linked Data
ClinVar Variation Id:
376736
ClinVar RCV Id:
RCV000428828
dbSNP Id:
rs1057520035
PubMed:
PMID:16731599
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54727438_54727439delinsTT , CM000666.2:g.54727438_54727439delinsTT | GRCh38 |
| NC_000004.11:g.55593604_55593605delinsTT , CM000666.1:g.55593604_55593605delinsTT | GRCh37 |
| NC_000004.10:g.55288361_55288362delinsTT | NCBI36 |
| NG_007456.1:g.74444_74445delinsTT , LRG_307:g.74444_74445delinsTT |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000412167.7:c.1661_1662delinsTT | ENSP00000390987.3:p.Trp554Phe | |
| ENST00000685269.1:n.1748_1749delinsTT | ||
| ENST00000686011.1:c.1658_1659delinsTT | ENSP00000509704.1:p.Trp553Phe | |
| ENST00000687109.1:c.1673_1674delinsTT | ENSP00000509371.1:p.Trp558Phe | |
| ENST00000687208.1:n.2085_2086delinsTT | ||
| ENST00000687246.1:c.1658_1659delinsTT | ENSP00000509114.1:p.Trp553Phe | |
| ENST00000687265.1:n.1828_1829delinsTT | ||
| ENST00000687295.1:c.1658_1659delinsTT | ENSP00000509450.1:p.Trp553Phe | |
| ENST00000689832.1:c.1673_1674delinsTT | ENSP00000509084.1:p.Trp558Phe | |
| ENST00000689994.1:c.1160_1161delinsTT | ENSP00000509156.1:p.Trp387Phe | |
| ENST00000690543.1:c.1661_1662delinsTT | ENSP00000508831.1:p.Trp554Phe | |
| ENST00000690917.1:n.1888_1889delinsTT | ||
| ENST00000691361.1:n.580_581delinsTT | ||
| ENST00000692783.1:c.1670_1671delinsTT | ENSP00000508733.1:p.Trp557Phe | |
| ENST00000692991.1:n.1767_1768delinsTT | ||
| ENST00000288135.6:c.1670_1671delinsTT MANE Select | ENSP00000288135.6:p.Trp557Phe | |
| ENST00000288135.5:c.1670_1671delinsTT | ENSP00000288135.5:p.Trp557Phe | |
| ENST00000412167.6:c.1658_1659delinsTT | ENSP00000390987.2:p.Trp553Phe | |
| NM_000222.2:c.1670_1671delinsTT , LRG_307t1:c.1670_1671delinsTT | NP_000213.1:p.Trp557Phe | |
| NM_001093772.1:c.1658_1659delinsTT | NP_001087241.1:p.Trp553Phe | |
| XM_005265740.1:c.1673_1674delinsTT | XP_005265797.1:p.Trp558Phe | |
| XM_005265741.1:c.1673_1674delinsTT | XP_005265798.1:p.Trp558Phe | |
| XM_005265742.1:c.1661_1662delinsTT | XP_005265799.1:p.Trp554Phe | |
| XM_005265742.3:c.1661_1662delinsTT | XP_005265799.1:p.Trp554Phe | |
| XM_017008178.1:c.1670_1671delinsTT | XP_016863667.1:p.Trp557Phe | |
| XM_017008179.1:c.1661_1662delinsTT | XP_016863668.1:p.Trp554Phe | |
| XM_017008180.1:c.1658_1659delinsTT | XP_016863669.1:p.Trp553Phe | |
| NM_000222.3:c.1670_1671delinsTT MANE Select | NP_000213.1:p.Trp557Phe | |
| NM_001093772.2:c.1658_1659delinsTT | NP_001087241.1:p.Trp553Phe | |
| NM_001385284.1:c.1673_1674delinsTT | NP_001372213.1:p.Trp558Phe | |
| NM_001385285.1:c.1670_1671delinsTT | NP_001372214.1:p.Trp557Phe | |
| NM_001385286.1:c.1658_1659delinsTT | NP_001372215.1:p.Trp553Phe | |
| NM_001385288.1:c.1661_1662delinsTT | NP_001372217.1:p.Trp554Phe | |
| NM_001385290.1:c.1673_1674delinsTT | NP_001372219.1:p.Trp558Phe | |
| NM_001385292.1:c.1661_1662delinsTT | NP_001372221.1:p.Trp554Phe |