Canonical Allele Identifier: CA1708914461

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55154428_55154429delinsTG , CM000669.2:g.55154428_55154429delinsTG	GRCh38
NC_000007.13:g.55222121_55222122delinsTG , CM000669.1:g.55222121_55222122delinsTG	GRCh37
NC_000007.12:g.55189615_55189616delinsTG	NCBI36
NG_007726.3:g.140397_140398delinsTG , LRG_304:g.140397_140398delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.730+276_730+277delinsTG	ENSP00000413354.2:n.730+276_730+277delinsTG
ENST00000700144.1:n.1079+276_1079+277delinsTG
ENST00000344576.7:c.889+276_889+277delinsTG	ENSP00000345973.2:n.889+276_889+277delinsTG
ENST00000275493.7:c.889+276_889+277delinsTG MANE Select	ENSP00000275493.2:n.889+276_889+277delinsTG
ENST00000275493.6:c.889+276_889+277delinsTG	ENSP00000275493.2:n.889+276_889+277delinsTG
ENST00000342916.7:c.889+276_889+277delinsTG	ENSP00000342376.3:n.889+276_889+277delinsTG
ENST00000344576.6:c.889+276_889+277delinsTG	ENSP00000345973.2:n.889+276_889+277delinsTG
ENST00000420316.6:c.889+276_889+277delinsTG	ENSP00000413843.2:n.889+276_889+277delinsTG
ENST00000442591.5:c.889+276_889+277delinsTG	ENSP00000410031.1:n.889+276_889+277delinsTG
ENST00000454757.6:c.754+276_754+277delinsTG	ENSP00000395243.3:n.754+276_754+277delinsTG
ENST00000455089.5:c.754+276_754+277delinsTG	ENSP00000415559.1:n.754+276_754+277delinsTG
NM_005228.3:c.889+276_889+277delinsTG , LRG_304t1:c.889+276_889+277delinsTG	NP_005219.2:n.889+276_889+277delinsTG
NM_201282.1:c.889+276_889+277delinsTG	NP_958439.1:n.889+276_889+277delinsTG
NM_201283.1:c.889+276_889+277delinsTG	NP_958440.1:n.889+276_889+277delinsTG
NM_201284.1:c.889+276_889+277delinsTG	NP_958441.1:n.889+276_889+277delinsTG
NM_001346897.1:c.754+276_754+277delinsTG	NP_001333826.1:n.754+276_754+277delinsTG
NM_001346898.1:c.889+276_889+277delinsTG	NP_001333827.1:n.889+276_889+277delinsTG
NM_001346899.1:c.754+276_754+277delinsTG	NP_001333828.1:n.754+276_754+277delinsTG
NM_001346900.1:c.730+276_730+277delinsTG	NP_001333829.1:n.730+276_730+277delinsTG
NM_001346941.1:c.89-1402_89-1401delinsTG	NP_001333870.1:n.89-1402_89-1401delinsTG
NM_005228.4:c.889+276_889+277delinsTG	NP_005219.2:n.889+276_889+277delinsTG
NM_005228.5:c.889+276_889+277delinsTG MANE Select	NP_005219.2:n.889+276_889+277delinsTG
NM_001346897.2:c.754+276_754+277delinsTG	NP_001333826.1:n.754+276_754+277delinsTG
NM_001346898.2:c.889+276_889+277delinsTG	NP_001333827.1:n.889+276_889+277delinsTG
NM_001346900.2:c.730+276_730+277delinsTG	NP_001333829.1:n.730+276_730+277delinsTG
NM_001346941.2:c.89-1402_89-1401delinsTG	NP_001333870.1:n.89-1402_89-1401delinsTG
NM_201282.2:c.889+276_889+277delinsTG	NP_958439.1:n.889+276_889+277delinsTG
NM_201284.2:c.889+276_889+277delinsTG	NP_958441.1:n.889+276_889+277delinsTG
NM_001346899.2:c.754+276_754+277delinsTG	NP_001333828.1:n.754+276_754+277delinsTG
NM_201283.2:c.889+276_889+277delinsTG	NP_958440.1:n.889+276_889+277delinsTG