Canonical Allele Identifier: CA2682856147

Gene: EGFR

Linked Data

• gnomAD v4: 7-55200761-T-TCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55200761_55200762insCTG , CM000669.2:g.55200761_55200762insCTG	GRCh38
NC_000007.13:g.55268454_55268455insCTG , CM000669.1:g.55268454_55268455insCTG	GRCh37
NC_000007.12:g.55235948_55235949insCTG	NCBI36
NG_007726.3:g.186730_186731insCTG , LRG_304:g.186730_186731insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2787+348_2787+349insCTG	ENSP00000413354.2:n.2787+348_2787+349insCTG
ENST00000700145.1:c.900-4586_900-4585insCTG
ENST00000700146.1:n.690+348_690+349insCTG
ENST00000700147.1:n.189_190insCTG
ENST00000275493.7:c.2946+348_2946+349insCTG MANE Select	ENSP00000275493.2:n.2946+348_2946+349insCTG
ENST00000275493.6:c.2946+348_2946+349insCTG	ENSP00000275493.2:n.2946+348_2946+349insCTG
ENST00000442591.5:c.*28+27833_*28+27834insCTG	ENSP00000410031.1:n.*28+27833_*28+27834insCTG
ENST00000454757.6:c.2811+348_2811+349insCTG	ENSP00000395243.3:n.2811+348_2811+349insCTG
ENST00000455089.5:c.2811+348_2811+349insCTG	ENSP00000415559.1:n.2811+348_2811+349insCTG
ENST00000485503.1:n.624_625insCTG
NM_005228.3:c.2946+348_2946+349insCTG , LRG_304t1:c.2946+348_2946+349insCTG	NP_005219.2:n.2946+348_2946+349insCTG
NM_001346897.1:c.2811+348_2811+349insCTG	NP_001333826.1:n.2811+348_2811+349insCTG
NM_001346898.1:c.2946+348_2946+349insCTG	NP_001333827.1:n.2946+348_2946+349insCTG
NM_001346899.1:c.2811+348_2811+349insCTG	NP_001333828.1:n.2811+348_2811+349insCTG
NM_001346900.1:c.2787+348_2787+349insCTG	NP_001333829.1:n.2787+348_2787+349insCTG
NM_001346941.1:c.2145+348_2145+349insCTG	NP_001333870.1:n.2145+348_2145+349insCTG
NM_005228.4:c.2946+348_2946+349insCTG	NP_005219.2:n.2946+348_2946+349insCTG
NM_005228.5:c.2946+348_2946+349insCTG MANE Select	NP_005219.2:n.2946+348_2946+349insCTG
NM_001346897.2:c.2811+348_2811+349insCTG	NP_001333826.1:n.2811+348_2811+349insCTG
NM_001346898.2:c.2946+348_2946+349insCTG	NP_001333827.1:n.2946+348_2946+349insCTG
NM_001346900.2:c.2787+348_2787+349insCTG	NP_001333829.1:n.2787+348_2787+349insCTG
NM_001346941.2:c.2145+348_2145+349insCTG	NP_001333870.1:n.2145+348_2145+349insCTG
NM_001346899.2:c.2811+348_2811+349insCTG	NP_001333828.1:n.2811+348_2811+349insCTG