Canonical Allele Identifier: CA2682854238

Gene: EGFR EGFR-AS1

Linked Data

• gnomAD v4: 7-55180764-G-GCT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55180764_55180765insCT , CM000669.2:g.55180764_55180765insCT	GRCh38
NC_000007.13:g.55248457_55248458insCT , CM000669.1:g.55248457_55248458insCT	GRCh37
NC_000007.12:g.55215951_55215952insCT	NCBI36
NG_007726.3:g.166733_166734insCT , LRG_304:g.166733_166734insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2125-529_2125-528insCT (EGFR)	ENSP00000413354.2:n.2125-529_2125-528insCT
ENST00000700145.1:c.633-529_633-528insCT (EGFR)
ENST00000275493.7:c.2284-529_2284-528insCT (EGFR) MANE Select	ENSP00000275493.2:n.2284-529_2284-528insCT
ENST00000275493.6:c.2284-529_2284-528insCT (EGFR)	ENSP00000275493.2:n.2284-529_2284-528insCT
ENST00000442591.5:c.*28+7836_*28+7837insCT (EGFR)	ENSP00000410031.1:n.*28+7836_*28+7837insCT
ENST00000454757.6:c.2149-529_2149-528insCT (EGFR)	ENSP00000395243.3:n.2149-529_2149-528insCT
ENST00000455089.5:c.2149-529_2149-528insCT (EGFR)	ENSP00000415559.1:n.2149-529_2149-528insCT
NM_005228.3:c.2284-529_2284-528insCT , LRG_304t1:c.2284-529_2284-528insCT (EGFR)	NP_005219.2:n.2284-529_2284-528insCT
NR_047551.1:n.1806_1807insAG (EGFR-AS1)
NM_001346897.1:c.2149-529_2149-528insCT (EGFR)	NP_001333826.1:n.2149-529_2149-528insCT
NM_001346898.1:c.2284-529_2284-528insCT (EGFR)	NP_001333827.1:n.2284-529_2284-528insCT
NM_001346899.1:c.2149-529_2149-528insCT (EGFR)	NP_001333828.1:n.2149-529_2149-528insCT
NM_001346900.1:c.2125-529_2125-528insCT (EGFR)	NP_001333829.1:n.2125-529_2125-528insCT
NM_001346941.1:c.1483-529_1483-528insCT (EGFR)	NP_001333870.1:n.1483-529_1483-528insCT
NM_005228.4:c.2284-529_2284-528insCT (EGFR)	NP_005219.2:n.2284-529_2284-528insCT
NM_005228.5:c.2284-529_2284-528insCT (EGFR) MANE Select	NP_005219.2:n.2284-529_2284-528insCT
NM_001346897.2:c.2149-529_2149-528insCT (EGFR)	NP_001333826.1:n.2149-529_2149-528insCT
NM_001346898.2:c.2284-529_2284-528insCT (EGFR)	NP_001333827.1:n.2284-529_2284-528insCT
NM_001346900.2:c.2125-529_2125-528insCT (EGFR)	NP_001333829.1:n.2125-529_2125-528insCT
NM_001346941.2:c.1483-529_1483-528insCT (EGFR)	NP_001333870.1:n.1483-529_1483-528insCT
NM_001346899.2:c.2149-529_2149-528insCT (EGFR)	NP_001333828.1:n.2149-529_2149-528insCT