Linked Data
ClinVar Variation Id:
45252
ClinVar RCV Id:
RCV000038408
dbSNP Id:
rs397517108
MyVariant Identifiers:
chr7:g.55249005_55249006delinsTT (hg19)
chr7:g.55181312_55181313delinsTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.55181312_55181313delinsTT , CM000669.2:g.55181312_55181313delinsTT | GRCh38 |
| NC_000007.13:g.55249005_55249006delinsTT , CM000669.1:g.55249005_55249006delinsTT | GRCh37 |
| NC_000007.12:g.55216499_55216500delinsTT | NCBI36 |
| NG_007726.3:g.167281_167282delinsTT , LRG_304:g.167281_167282delinsTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450046.2:c.2144_2145delinsTT (EGFR) | ENSP00000413354.2:p.Ser715Ile | |
| ENST00000700145.1:c.652_653delinsTT (EGFR) | ||
| ENST00000275493.7:c.2303_2304delinsTT (EGFR) MANE Select | ENSP00000275493.2:p.Ser768Ile | |
| ENST00000275493.6:c.2303_2304delinsTT (EGFR) | ENSP00000275493.2:p.Ser768Ile | |
| ENST00000442591.5:c.*28+8384_*28+8385delinsTT (EGFR) | ENSP00000410031.1:n.*28+8384_*28+8385delinsTT | |
| ENST00000454757.6:c.2168_2169delinsTT (EGFR) | ENSP00000395243.3:p.Ser723Ile | |
| ENST00000455089.5:c.2168_2169delinsTT (EGFR) | ENSP00000415559.1:p.Ser723Ile | |
| NM_005228.3:c.2303_2304delinsTT , LRG_304t1:c.2303_2304delinsTT (EGFR) | NP_005219.2:p.Ser768Ile | |
| NR_047551.1:n.1258_1259delinsAA (EGFR-AS1) | ||
| NM_001346897.1:c.2168_2169delinsTT (EGFR) | NP_001333826.1:p.Ser723Ile | |
| NM_001346898.1:c.2303_2304delinsTT (EGFR) | NP_001333827.1:p.Ser768Ile | |
| NM_001346899.1:c.2168_2169delinsTT (EGFR) | NP_001333828.1:p.Ser723Ile | |
| NM_001346900.1:c.2144_2145delinsTT (EGFR) | NP_001333829.1:p.Ser715Ile | |
| NM_001346941.1:c.1502_1503delinsTT (EGFR) | NP_001333870.1:p.Ser501Ile | |
| NM_005228.4:c.2303_2304delinsTT (EGFR) | NP_005219.2:p.Ser768Ile | |
| NM_005228.5:c.2303_2304delinsTT (EGFR) MANE Select | NP_005219.2:p.Ser768Ile | |
| NM_001346897.2:c.2168_2169delinsTT (EGFR) | NP_001333826.1:p.Ser723Ile | |
| NM_001346898.2:c.2303_2304delinsTT (EGFR) | NP_001333827.1:p.Ser768Ile | |
| NM_001346900.2:c.2144_2145delinsTT (EGFR) | NP_001333829.1:p.Ser715Ile | |
| NM_001346941.2:c.1502_1503delinsTT (EGFR) | NP_001333870.1:p.Ser501Ile | |
| NM_001346899.2:c.2168_2169delinsTT (EGFR) | NP_001333828.1:p.Ser723Ile |