Canonical Allele Identifier: CA1708922456

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191747_55191748delinsTG , CM000669.2:g.55191747_55191748delinsTG	GRCh38
NC_000007.13:g.55259440_55259441delinsTG , CM000669.1:g.55259440_55259441delinsTG	GRCh37
NC_000007.12:g.55226934_55226935delinsTG	NCBI36
NG_007726.3:g.177716_177717delinsTG , LRG_304:g.177716_177717delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2339_2340delinsTG	ENSP00000413354.2:p.Leu780=
ENST00000700145.1:c.847_848delinsTG
ENST00000275493.7:c.2498_2499delinsTG MANE Select	ENSP00000275493.2:p.Leu833=
ENST00000275493.6:c.2498_2499delinsTG	ENSP00000275493.2:p.Leu833=
ENST00000442591.5:c.*28+18819_*28+18820delinsTG	ENSP00000410031.1:n.*28+18819_*28+18820de...
ENST00000454757.6:c.2363_2364delinsTG	ENSP00000395243.3:p.Leu788=
ENST00000455089.5:c.2363_2364delinsTG	ENSP00000415559.1:p.Leu788=
NM_005228.3:c.2498_2499delinsTG , LRG_304t1:c.2498_2499delinsTG	NP_005219.2:p.Leu833=
NM_001346897.1:c.2363_2364delinsTG	NP_001333826.1:p.Leu788=
NM_001346898.1:c.2498_2499delinsTG	NP_001333827.1:p.Leu833=
NM_001346899.1:c.2363_2364delinsTG	NP_001333828.1:p.Leu788=
NM_001346900.1:c.2339_2340delinsTG	NP_001333829.1:p.Leu780=
NM_001346941.1:c.1697_1698delinsTG	NP_001333870.1:p.Leu566=
NM_005228.4:c.2498_2499delinsTG	NP_005219.2:p.Leu833=
NM_005228.5:c.2498_2499delinsTG MANE Select	NP_005219.2:p.Leu833=
NM_001346897.2:c.2363_2364delinsTG	NP_001333826.1:p.Leu788=
NM_001346898.2:c.2498_2499delinsTG	NP_001333827.1:p.Leu833=
NM_001346900.2:c.2339_2340delinsTG	NP_001333829.1:p.Leu780=
NM_001346941.2:c.1697_1698delinsTG	NP_001333870.1:p.Leu566=
NM_001346899.2:c.2363_2364delinsTG	NP_001333828.1:p.Leu788=