Linked Data
ClinVar Variation Id:
2656398
ClinVar RCV Id:
RCV003431747
dbSNP Id:
rs9281379
ExAC:
6:31324601 C / CA
gnomAD v2:
6-31324601-C-CA
gnomAD v3:
6-31356824-C-CA
gnomAD v4:
6-31356824-C-CA
COSMIC:
COSM297186
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31356824_31356825insA , CM000668.2:g.31356824_31356825insA | GRCh38 |
| NC_000006.11:g.31324601_31324602insA , CM000668.1:g.31324601_31324602insA | GRCh37 |
| NC_000006.10:g.31432580_31432581insA | NCBI36 |
| NG_023187.1:g.5388_5389insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.1679_1680insT | ||
| ENST00000481849.6:n.1679_1680insT | ||
| ENST00000497377.6:n.1679_1680insT | ||
| ENST00000640094.2:c.206_207insT | ENSP00000491275.2:p.Glu69AspfsTer30 | |
| ENST00000696558.1:c.206_207insT | ENSP00000512716.1:p.Glu69AspfsTer30 | |
| ENST00000696559.1:c.206_207insT | ENSP00000512717.1:p.Glu69AspfsTer30 | |
| ENST00000696560.1:c.206_207insT | ENSP00000512718.1:p.Glu69AspfsTer30 | |
| ENST00000696561.1:c.206_207insT | ENSP00000512719.1:p.Glu69AspfsTer30 | |
| ENST00000696562.1:c.206_207insT | ENSP00000512720.1:p.Glu69AspfsTer30 | |
| ENST00000412585.7:c.206_207insT MANE Select | ENSP00000399168.2:p.Glu69AspfsTer30 | |
| ENST00000412585.6:c.206_207insT | ENSP00000399168.2:p.Glu69AspfsTer30 | |
| ENST00000434333.1:c.239_240insT | ENSP00000405931.1:p.Glu80AspfsTer30 | |
| ENST00000474381.1:n.81_82insT | ||
| ENST00000498007.1:n.227_228insT | ||
| ENST00000603274.1:n.178_179insA | ||
| NM_005514.6:c.206_207insT | NP_005505.2:p.Glu69AspfsTer30 | |
| XM_011514556.1:c.239_240insT | XP_011512858.1:p.Glu80AspfsTer30 | |
| XM_011514557.1:c.206_207insT | XP_011512859.1:p.Glu69AspfsTer30 | |
| XR_926175.1:n.216_217insT | ||
| NM_005514.7:c.206_207insT | NP_005505.2:p.Glu69AspfsTer30 | |
| NM_005514.8:c.206_207insT MANE Select | NP_005505.2:p.Glu69AspfsTer30 |