Canonical Allele Identifier: CA3260261262

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191755_55191757del , CM000669.2:g.55191755_55191757del	GRCh38
NC_000007.13:g.55259448_55259450del , CM000669.1:g.55259448_55259450del	GRCh37
NC_000007.12:g.55226942_55226944del	NCBI36
NG_007726.3:g.177724_177726del , LRG_304:g.177724_177726del

Transcript Alleles

HGVS	Amino-acid Change
NM_005228.5:c.2506_2508del MANE Select	NP_005219.2:p.Arg836del
ENST00000275493.7:c.2506_2508del MANE Select	ENSP00000275493.2:p.Arg836del
NM_001346897.1:c.2371_2373del	NP_001333826.1:p.Arg791del
NM_001346897.2:c.2371_2373del	NP_001333826.1:p.Arg791del
NM_001346898.1:c.2506_2508del	NP_001333827.1:p.Arg836del
NM_001346898.2:c.2506_2508del	NP_001333827.1:p.Arg836del
NM_001346899.1:c.2371_2373del	NP_001333828.1:p.Arg791del
NM_001346899.2:c.2371_2373del	NP_001333828.1:p.Arg791del
NM_001346900.1:c.2347_2349del	NP_001333829.1:p.Arg783del
NM_001346900.2:c.2347_2349del	NP_001333829.1:p.Arg783del
NM_001346941.1:c.1705_1707del	NP_001333870.1:p.Arg569del
NM_001346941.2:c.1705_1707del	NP_001333870.1:p.Arg569del
NM_005228.3:c.2506_2508del , LRG_304t1:c.2506_2508del	NP_005219.2:p.Arg836del
NM_005228.4:c.2506_2508del	NP_005219.2:p.Arg836del
ENST00000275493.6:c.2506_2508del	ENSP00000275493.2:p.Arg836del
ENST00000442591.5:c.*28+18827_*28+18829del	ENSP00000410031.1:n.*28+18827_*28+18829del
ENST00000450046.2:c.2347_2349del	ENSP00000413354.2:p.Arg783del
ENST00000454757.6:c.2371_2373del	ENSP00000395243.3:p.Arg791del
ENST00000455089.5:c.2371_2373del	ENSP00000415559.1:p.Arg791del
ENST00000700145.1:c.855_857del