Canonical Allele Identifier: CA1708914395

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55154366_55154367delinsTG , CM000669.2:g.55154366_55154367delinsTG	GRCh38
NC_000007.13:g.55222059_55222060delinsTG , CM000669.1:g.55222059_55222060delinsTG	GRCh37
NC_000007.12:g.55189553_55189554delinsTG	NCBI36
NG_007726.3:g.140335_140336delinsTG , LRG_304:g.140335_140336delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.730+214_730+215delinsTG	ENSP00000413354.2:n.730+214_730+215delinsTG
ENST00000700144.1:n.1079+214_1079+215delinsTG
ENST00000344576.7:c.889+214_889+215delinsTG	ENSP00000345973.2:n.889+214_889+215delinsTG
ENST00000275493.7:c.889+214_889+215delinsTG MANE Select	ENSP00000275493.2:n.889+214_889+215delinsTG
ENST00000275493.6:c.889+214_889+215delinsTG	ENSP00000275493.2:n.889+214_889+215delinsTG
ENST00000342916.7:c.889+214_889+215delinsTG	ENSP00000342376.3:n.889+214_889+215delinsTG
ENST00000344576.6:c.889+214_889+215delinsTG	ENSP00000345973.2:n.889+214_889+215delinsTG
ENST00000420316.6:c.889+214_889+215delinsTG	ENSP00000413843.2:n.889+214_889+215delinsTG
ENST00000442591.5:c.889+214_889+215delinsTG	ENSP00000410031.1:n.889+214_889+215delinsTG
ENST00000454757.6:c.754+214_754+215delinsTG	ENSP00000395243.3:n.754+214_754+215delinsTG
ENST00000455089.5:c.754+214_754+215delinsTG	ENSP00000415559.1:n.754+214_754+215delinsTG
NM_005228.3:c.889+214_889+215delinsTG , LRG_304t1:c.889+214_889+215delinsTG	NP_005219.2:n.889+214_889+215delinsTG
NM_201282.1:c.889+214_889+215delinsTG	NP_958439.1:n.889+214_889+215delinsTG
NM_201283.1:c.889+214_889+215delinsTG	NP_958440.1:n.889+214_889+215delinsTG
NM_201284.1:c.889+214_889+215delinsTG	NP_958441.1:n.889+214_889+215delinsTG
NM_001346897.1:c.754+214_754+215delinsTG	NP_001333826.1:n.754+214_754+215delinsTG
NM_001346898.1:c.889+214_889+215delinsTG	NP_001333827.1:n.889+214_889+215delinsTG
NM_001346899.1:c.754+214_754+215delinsTG	NP_001333828.1:n.754+214_754+215delinsTG
NM_001346900.1:c.730+214_730+215delinsTG	NP_001333829.1:n.730+214_730+215delinsTG
NM_001346941.1:c.89-1464_89-1463delinsTG	NP_001333870.1:n.89-1464_89-1463delinsTG
NM_005228.4:c.889+214_889+215delinsTG	NP_005219.2:n.889+214_889+215delinsTG
NM_005228.5:c.889+214_889+215delinsTG MANE Select	NP_005219.2:n.889+214_889+215delinsTG
NM_001346897.2:c.754+214_754+215delinsTG	NP_001333826.1:n.754+214_754+215delinsTG
NM_001346898.2:c.889+214_889+215delinsTG	NP_001333827.1:n.889+214_889+215delinsTG
NM_001346900.2:c.730+214_730+215delinsTG	NP_001333829.1:n.730+214_730+215delinsTG
NM_001346941.2:c.89-1464_89-1463delinsTG	NP_001333870.1:n.89-1464_89-1463delinsTG
NM_201282.2:c.889+214_889+215delinsTG	NP_958439.1:n.889+214_889+215delinsTG
NM_201284.2:c.889+214_889+215delinsTG	NP_958441.1:n.889+214_889+215delinsTG
NM_001346899.2:c.754+214_754+215delinsTG	NP_001333828.1:n.754+214_754+215delinsTG
NM_201283.2:c.889+214_889+215delinsTG	NP_958440.1:n.889+214_889+215delinsTG