Linked Data
ClinVar Variation Id:
45259
ClinVar RCV Id:
RCV000038415
dbSNP Id:
rs397517113
MyVariant Identifiers:
chr7:g.55249015_55249023dupCCCCCACGT (hg19)
chr7:g.55181322_55181330dupCCCCCACGT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.55181322_55181330dup , CM000669.2:g.55181322_55181330dup | GRCh38 |
| NC_000007.13:g.55249015_55249023dup , CM000669.1:g.55249015_55249023dup | GRCh37 |
| NC_000007.12:g.55216509_55216517dup | NCBI36 |
| NG_007726.3:g.167291_167299dup , LRG_304:g.167291_167299dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450046.2:c.2154_2162dup (EGFR) | ENSP00000413354.2:p.Val721_Cys722insProHisVal | |
| ENST00000700145.1:c.662_670dup (EGFR) | ||
| ENST00000275493.7:c.2313_2321dup (EGFR) MANE Select | ENSP00000275493.2:p.Val774_Cys775insProHisVal | |
| ENST00000275493.6:c.2313_2321dup (EGFR) | ENSP00000275493.2:p.Val774_Cys775insProHisVal | |
| ENST00000442591.5:c.*28+8394_*28+8402dup (EGFR) | ENSP00000410031.1:n.*28+8394_*28+8402dup | |
| ENST00000454757.6:c.2178_2186dup (EGFR) | ENSP00000395243.3:p.Val729_Cys730insProHisVal | |
| ENST00000455089.5:c.2178_2186dup (EGFR) | ENSP00000415559.1:p.Val729_Cys730insProHisVal | |
| NM_005228.3:c.2313_2321dup , LRG_304t1:c.2313_2321dup (EGFR) | NP_005219.2:p.Val774_Cys775insProHisVal | |
| NR_047551.1:n.1241_1249dup (EGFR-AS1) | ||
| NM_001346897.1:c.2178_2186dup (EGFR) | NP_001333826.1:p.Val729_Cys730insProHisVal | |
| NM_001346898.1:c.2313_2321dup (EGFR) | NP_001333827.1:p.Val774_Cys775insProHisVal | |
| NM_001346899.1:c.2178_2186dup (EGFR) | NP_001333828.1:p.Val729_Cys730insProHisVal | |
| NM_001346900.1:c.2154_2162dup (EGFR) | NP_001333829.1:p.Val721_Cys722insProHisVal | |
| NM_001346941.1:c.1512_1520dup (EGFR) | NP_001333870.1:p.Val507_Cys508insProHisVal | |
| NM_005228.4:c.2313_2321dup (EGFR) | NP_005219.2:p.Val774_Cys775insProHisVal | |
| NM_005228.5:c.2313_2321dup (EGFR) MANE Select | NP_005219.2:p.Val774_Cys775insProHisVal | |
| NM_001346897.2:c.2178_2186dup (EGFR) | NP_001333826.1:p.Val729_Cys730insProHisVal | |
| NM_001346898.2:c.2313_2321dup (EGFR) | NP_001333827.1:p.Val774_Cys775insProHisVal | |
| NM_001346900.2:c.2154_2162dup (EGFR) | NP_001333829.1:p.Val721_Cys722insProHisVal | |
| NM_001346941.2:c.1512_1520dup (EGFR) | NP_001333870.1:p.Val507_Cys508insProHisVal | |
| NM_001346899.2:c.2178_2186dup (EGFR) | NP_001333828.1:p.Val729_Cys730insProHisVal |