Canonical Allele Identifier: CA2775503197

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55125326_55125327del , CM000669.2:g.55125326_55125327del	GRCh38
NC_000007.13:g.55193019_55193020del , CM000669.1:g.55193019_55193020del	GRCh37
NC_000007.12:g.55160513_55160514del	NCBI36
NG_007726.3:g.111295_111296del , LRG_304:g.111295_111296del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.-72+15368_-72+15369del	ENSP00000413354.2:n.-72+15368_-72+15369del
ENST00000700144.1:n.279-16960_279-16959del
ENST00000344576.7:c.89-16960_89-16959del	ENSP00000345973.2:n.89-16960_89-16959del
ENST00000275493.7:c.89-16960_89-16959del MANE Select	ENSP00000275493.2:n.89-16960_89-16959del
ENST00000275493.6:c.89-16960_89-16959del	ENSP00000275493.2:n.89-16960_89-16959del
ENST00000342916.7:c.89-16960_89-16959del	ENSP00000342376.3:n.89-16960_89-16959del
ENST00000344576.6:c.89-16960_89-16959del	ENSP00000345973.2:n.89-16960_89-16959del
ENST00000420316.6:c.89-16960_89-16959del	ENSP00000413843.2:n.89-16960_89-16959del
ENST00000442591.5:c.89-16960_89-16959del	ENSP00000410031.1:n.89-16960_89-16959del
ENST00000450046.1:c.-72+15368_-72+15369del	ENSP00000413354.1:n.-72+15368_-72+15369del
ENST00000454757.6:c.89-16960_89-16959del	ENSP00000395243.3:n.89-16960_89-16959del
ENST00000455089.5:c.89-16960_89-16959del	ENSP00000415559.1:n.89-16960_89-16959del
NM_005228.3:c.89-16960_89-16959del , LRG_304t1:c.89-16960_89-16959del	NP_005219.2:n.89-16960_89-16959del
NM_201282.1:c.89-16960_89-16959del	NP_958439.1:n.89-16960_89-16959del
NM_201283.1:c.89-16960_89-16959del	NP_958440.1:n.89-16960_89-16959del
NM_201284.1:c.89-16960_89-16959del	NP_958441.1:n.89-16960_89-16959del
NM_001346897.1:c.89-16960_89-16959del	NP_001333826.1:n.89-16960_89-16959del
NM_001346898.1:c.89-16960_89-16959del	NP_001333827.1:n.89-16960_89-16959del
NM_001346899.1:c.89-16960_89-16959del	NP_001333828.1:n.89-16960_89-16959del
NM_001346900.1:c.-72+15368_-72+15369del	NP_001333829.1:n.-72+15368_-72+15369del
NM_001346941.1:c.89-30504_89-30503del	NP_001333870.1:n.89-30504_89-30503del
NM_005228.4:c.89-16960_89-16959del	NP_005219.2:n.89-16960_89-16959del
NM_005228.5:c.89-16960_89-16959del MANE Select	NP_005219.2:n.89-16960_89-16959del
NM_001346897.2:c.89-16960_89-16959del	NP_001333826.1:n.89-16960_89-16959del
NM_001346898.2:c.89-16960_89-16959del	NP_001333827.1:n.89-16960_89-16959del
NM_001346900.2:c.-72+15368_-72+15369del	NP_001333829.1:n.-72+15368_-72+15369del
NM_001346941.2:c.89-30504_89-30503del	NP_001333870.1:n.89-30504_89-30503del
NM_201282.2:c.89-16960_89-16959del	NP_958439.1:n.89-16960_89-16959del
NM_201284.2:c.89-16960_89-16959del	NP_958441.1:n.89-16960_89-16959del
NM_001346899.2:c.89-16960_89-16959del	NP_001333828.1:n.89-16960_89-16959del
NM_201283.2:c.89-16960_89-16959del	NP_958440.1:n.89-16960_89-16959del