Canonical Allele Identifier: CA135863
Gene: EGFR HGNC NCBI
EGFR-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55181324_55181329dup , CM000669.2:g.55181324_55181329dup GRCh38
NC_000007.13:g.55249017_55249022dup , CM000669.1:g.55249017_55249022dup GRCh37
NC_000007.12:g.55216511_55216516dup NCBI36
NG_007726.3:g.167293_167298dup , LRG_304:g.167293_167298dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000450046.2:c.2156_2161dup (EGFR) ENSP00000413354.2:p.His720_Val721insAlaHis
ENST00000700145.1:c.664_669dup (EGFR)
ENST00000275493.7:c.2315_2320dup (EGFR) MANE Select ENSP00000275493.2:p.His773_Val774insAlaHis
ENST00000275493.6:c.2315_2320dup (EGFR) ENSP00000275493.2:p.His773_Val774insAlaHis
ENST00000442591.5:c.*28+8396_*28+8401dup (EGFR) ENSP00000410031.1:n.*28+8396_*28+8401dup
ENST00000454757.6:c.2180_2185dup (EGFR) ENSP00000395243.3:p.His728_Val729insAlaHis
ENST00000455089.5:c.2180_2185dup (EGFR) ENSP00000415559.1:p.His728_Val729insAlaHis
NM_005228.3:c.2315_2320dup , LRG_304t1:c.2315_2320dup (EGFR) NP_005219.2:p.His773_Val774insAlaHis
NR_047551.1:n.1242_1247dup (EGFR-AS1)
NM_001346897.1:c.2180_2185dup (EGFR) NP_001333826.1:p.His728_Val729insAlaHis
NM_001346898.1:c.2315_2320dup (EGFR) NP_001333827.1:p.His773_Val774insAlaHis
NM_001346899.1:c.2180_2185dup (EGFR) NP_001333828.1:p.His728_Val729insAlaHis
NM_001346900.1:c.2156_2161dup (EGFR) NP_001333829.1:p.His720_Val721insAlaHis
NM_001346941.1:c.1514_1519dup (EGFR) NP_001333870.1:p.His506_Val507insAlaHis
NM_005228.4:c.2315_2320dup (EGFR) NP_005219.2:p.His773_Val774insAlaHis
NM_005228.5:c.2315_2320dup (EGFR) MANE Select NP_005219.2:p.His773_Val774insAlaHis
NM_001346897.2:c.2180_2185dup (EGFR) NP_001333826.1:p.His728_Val729insAlaHis
NM_001346898.2:c.2315_2320dup (EGFR) NP_001333827.1:p.His773_Val774insAlaHis
NM_001346900.2:c.2156_2161dup (EGFR) NP_001333829.1:p.His720_Val721insAlaHis
NM_001346941.2:c.1514_1519dup (EGFR) NP_001333870.1:p.His506_Val507insAlaHis
NM_001346899.2:c.2180_2185dup (EGFR) NP_001333828.1:p.His728_Val729insAlaHis