Canonical Allele Identifier: CA1708918305
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174768_55174786delinsTCAAGGAATTAAGAGAAGC , CM000669.2:g.55174768_55174786delinsTCAAGGAATTAAGAGAAGC GRCh38
NC_000007.13:g.55242461_55242479delinsTCAAGGAATTAAGAGAAGC , CM000669.1:g.55242461_55242479delinsTCAAGGAATTAAGAGAAGC GRCh37
NC_000007.12:g.55209955_55209973delinsTCAAGGAATTAAGAGAAGC NCBI36
NG_007726.3:g.160737_160755delinsTCAAGGAATTAAGAGAAGC , LRG_304:g.160737_160755delinsTCAAGGAATTAAGAGAAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.2231_2249delinsTCAAGGAATTAAGAGAAGC MANE Select ENSP00000275493.2:p.Ile744=
ENST00000275493.6:c.2231_2249delinsTCAAGGAATTAAGAGAAGC ENSP00000275493.2:p.Ile744=
ENST00000442591.5:c.*28+1840_*28+1858delinsTCAAGGAATTAAGAGAAGC ENSP00000410031.1:p.=
ENST00000454757.6:c.2096_2114delinsTCAAGGAATTAAGAGAAGC ENSP00000395243.3:p.Ile699=
ENST00000455089.5:c.2096_2114delinsTCAAGGAATTAAGAGAAGC ENSP00000415559.1:p.Ile699=
NM_005228.3:c.2231_2249delinsTCAAGGAATTAAGAGAAGC , LRG_304t1:c.2231_2249delinsTCAAGGAATTAAGAGAAGC NP_005219.2:p.Ile744=
NM_001346897.1:c.2096_2114delinsTCAAGGAATTAAGAGAAGC NP_001333826.1:p.Ile699=
NM_001346898.1:c.2231_2249delinsTCAAGGAATTAAGAGAAGC NP_001333827.1:p.Ile744=
NM_001346899.1:c.2096_2114delinsTCAAGGAATTAAGAGAAGC NP_001333828.1:p.Ile699=
NM_001346900.1:c.2072_2090delinsTCAAGGAATTAAGAGAAGC NP_001333829.1:p.Ile691=
NM_001346941.1:c.1430_1448delinsTCAAGGAATTAAGAGAAGC NP_001333870.1:p.Ile477=
NM_005228.4:c.2231_2249delinsTCAAGGAATTAAGAGAAGC NP_005219.2:p.Ile744=
NM_005228.5:c.2231_2249delinsTCAAGGAATTAAGAGAAGC MANE Select NP_005219.2:p.Ile744=
NM_001346897.2:c.2096_2114delinsTCAAGGAATTAAGAGAAGC NP_001333826.1:p.Ile699=
NM_001346898.2:c.2231_2249delinsTCAAGGAATTAAGAGAAGC NP_001333827.1:p.Ile744=
NM_001346900.2:c.2072_2090delinsTCAAGGAATTAAGAGAAGC NP_001333829.1:p.Ile691=
NM_001346941.2:c.1430_1448delinsTCAAGGAATTAAGAGAAGC NP_001333870.1:p.Ile477=
NM_001346899.2:c.2096_2114delinsTCAAGGAATTAAGAGAAGC NP_001333828.1:p.Ile699=