Canonical Allele Identifier: CA2573051279

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191749_55191751delinsATT , CM000669.2:g.55191749_55191751delinsATT	GRCh38
NC_000007.13:g.55259442_55259444delinsATT , CM000669.1:g.55259442_55259444delinsATT	GRCh37
NC_000007.12:g.55226936_55226938delinsATT	NCBI36
NG_007726.3:g.177718_177720delinsATT , LRG_304:g.177718_177720delinsATT

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2341_2343delinsATT	ENSP00000413354.2:p.Val781Ile
ENST00000700145.1:c.849_851delinsATT
ENST00000275493.7:c.2500_2502delinsATT MANE Select	ENSP00000275493.2:p.Val834Ile
ENST00000275493.6:c.2500_2502delinsATT	ENSP00000275493.2:p.Val834Ile
ENST00000442591.5:c.*28+18821_*28+18823delinsATT	ENSP00000410031.1:n.*28+18821_*28+18823de...
ENST00000454757.6:c.2365_2367delinsATT	ENSP00000395243.3:p.Val789Ile
ENST00000455089.5:c.2365_2367delinsATT	ENSP00000415559.1:p.Val789Ile
NM_005228.3:c.2500_2502delinsATT , LRG_304t1:c.2500_2502delinsATT	NP_005219.2:p.Val834Ile
NM_001346897.1:c.2365_2367delinsATT	NP_001333826.1:p.Val789Ile
NM_001346898.1:c.2500_2502delinsATT	NP_001333827.1:p.Val834Ile
NM_001346899.1:c.2365_2367delinsATT	NP_001333828.1:p.Val789Ile
NM_001346900.1:c.2341_2343delinsATT	NP_001333829.1:p.Val781Ile
NM_001346941.1:c.1699_1701delinsATT	NP_001333870.1:p.Val567Ile
NM_005228.4:c.2500_2502delinsATT	NP_005219.2:p.Val834Ile
NM_005228.5:c.2500_2502delinsATT MANE Select	NP_005219.2:p.Val834Ile
NM_001346897.2:c.2365_2367delinsATT	NP_001333826.1:p.Val789Ile
NM_001346898.2:c.2500_2502delinsATT	NP_001333827.1:p.Val834Ile
NM_001346900.2:c.2341_2343delinsATT	NP_001333829.1:p.Val781Ile
NM_001346941.2:c.1699_1701delinsATT	NP_001333870.1:p.Val567Ile
NM_001346899.2:c.2365_2367delinsATT	NP_001333828.1:p.Val789Ile