Canonical Allele Identifier: CA1708914508

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55154477_55154478delinsAG , CM000669.2:g.55154477_55154478delinsAG	GRCh38
NC_000007.13:g.55222170_55222171delinsAG , CM000669.1:g.55222170_55222171delinsAG	GRCh37
NC_000007.12:g.55189664_55189665delinsAG	NCBI36
NG_007726.3:g.140446_140447delinsAG , LRG_304:g.140446_140447delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.730+325_730+326delinsAG	ENSP00000413354.2:n.730+325_730+326delinsAG
ENST00000700144.1:n.1079+325_1079+326delinsAG
ENST00000344576.7:c.889+325_889+326delinsAG	ENSP00000345973.2:n.889+325_889+326delinsAG
ENST00000275493.7:c.889+325_889+326delinsAG MANE Select	ENSP00000275493.2:n.889+325_889+326delinsAG
ENST00000275493.6:c.889+325_889+326delinsAG	ENSP00000275493.2:n.889+325_889+326delinsAG
ENST00000342916.7:c.889+325_889+326delinsAG	ENSP00000342376.3:n.889+325_889+326delinsAG
ENST00000344576.6:c.889+325_889+326delinsAG	ENSP00000345973.2:n.889+325_889+326delinsAG
ENST00000420316.6:c.889+325_889+326delinsAG	ENSP00000413843.2:n.889+325_889+326delinsAG
ENST00000442591.5:c.889+325_889+326delinsAG	ENSP00000410031.1:n.889+325_889+326delinsAG
ENST00000454757.6:c.754+325_754+326delinsAG	ENSP00000395243.3:n.754+325_754+326delinsAG
ENST00000455089.5:c.754+325_754+326delinsAG	ENSP00000415559.1:n.754+325_754+326delinsAG
NM_005228.3:c.889+325_889+326delinsAG , LRG_304t1:c.889+325_889+326delinsAG	NP_005219.2:n.889+325_889+326delinsAG
NM_201282.1:c.889+325_889+326delinsAG	NP_958439.1:n.889+325_889+326delinsAG
NM_201283.1:c.889+325_889+326delinsAG	NP_958440.1:n.889+325_889+326delinsAG
NM_201284.1:c.889+325_889+326delinsAG	NP_958441.1:n.889+325_889+326delinsAG
NM_001346897.1:c.754+325_754+326delinsAG	NP_001333826.1:n.754+325_754+326delinsAG
NM_001346898.1:c.889+325_889+326delinsAG	NP_001333827.1:n.889+325_889+326delinsAG
NM_001346899.1:c.754+325_754+326delinsAG	NP_001333828.1:n.754+325_754+326delinsAG
NM_001346900.1:c.730+325_730+326delinsAG	NP_001333829.1:n.730+325_730+326delinsAG
NM_001346941.1:c.89-1353_89-1352delinsAG	NP_001333870.1:n.89-1353_89-1352delinsAG
NM_005228.4:c.889+325_889+326delinsAG	NP_005219.2:n.889+325_889+326delinsAG
NM_005228.5:c.889+325_889+326delinsAG MANE Select	NP_005219.2:n.889+325_889+326delinsAG
NM_001346897.2:c.754+325_754+326delinsAG	NP_001333826.1:n.754+325_754+326delinsAG
NM_001346898.2:c.889+325_889+326delinsAG	NP_001333827.1:n.889+325_889+326delinsAG
NM_001346900.2:c.730+325_730+326delinsAG	NP_001333829.1:n.730+325_730+326delinsAG
NM_001346941.2:c.89-1353_89-1352delinsAG	NP_001333870.1:n.89-1353_89-1352delinsAG
NM_201282.2:c.889+325_889+326delinsAG	NP_958439.1:n.889+325_889+326delinsAG
NM_201284.2:c.889+325_889+326delinsAG	NP_958441.1:n.889+325_889+326delinsAG
NM_001346899.2:c.754+325_754+326delinsAG	NP_001333828.1:n.754+325_754+326delinsAG
NM_201283.2:c.889+325_889+326delinsAG	NP_958440.1:n.889+325_889+326delinsAG