Canonical Allele Identifier: CA645561575

Gene: EGFR EGFR-AS1

Linked Data

• dbSNP Id: rs2128958352
• COSMIC: COSM1651745

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181317_55181325dup , CM000669.2:g.55181317_55181325dup	GRCh38
NC_000007.13:g.55249010_55249018dup , CM000669.1:g.55249010_55249018dup	GRCh37
NC_000007.12:g.55216504_55216512dup	NCBI36
NG_007726.3:g.167286_167294dup , LRG_304:g.167286_167294dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2149_2157dup (EGFR)	ENSP00000413354.2:p.Pro719_His720insAspAsnPro
ENST00000700145.1:c.657_665dup (EGFR)
ENST00000275493.7:c.2308_2316dup (EGFR) MANE Select	ENSP00000275493.2:p.Pro772_His773insAspAsnPro
ENST00000275493.6:c.2308_2316dup (EGFR)	ENSP00000275493.2:p.Pro772_His773insAspAsnPro
ENST00000442591.5:c.*28+8389_*28+8397dup (EGFR)	ENSP00000410031.1:n.*28+8389_*28+8397dup
ENST00000454757.6:c.2173_2181dup (EGFR)	ENSP00000395243.3:p.Pro727_His728insAspAsnPro
ENST00000455089.5:c.2173_2181dup (EGFR)	ENSP00000415559.1:p.Pro727_His728insAspAsnPro
NM_005228.3:c.2308_2316dup , LRG_304t1:c.2308_2316dup (EGFR)	NP_005219.2:p.Pro772_His773insAspAsnPro
NR_047551.1:n.1246_1254dup (EGFR-AS1)
NM_001346897.1:c.2173_2181dup (EGFR)	NP_001333826.1:p.Pro727_His728insAspAsnPro
NM_001346898.1:c.2308_2316dup (EGFR)	NP_001333827.1:p.Pro772_His773insAspAsnPro
NM_001346899.1:c.2173_2181dup (EGFR)	NP_001333828.1:p.Pro727_His728insAspAsnPro
NM_001346900.1:c.2149_2157dup (EGFR)	NP_001333829.1:p.Pro719_His720insAspAsnPro
NM_001346941.1:c.1507_1515dup (EGFR)	NP_001333870.1:p.Pro505_His506insAspAsnPro
NM_005228.4:c.2308_2316dup (EGFR)	NP_005219.2:p.Pro772_His773insAspAsnPro
NM_005228.5:c.2308_2316dup (EGFR) MANE Select	NP_005219.2:p.Pro772_His773insAspAsnPro
NM_001346897.2:c.2173_2181dup (EGFR)	NP_001333826.1:p.Pro727_His728insAspAsnPro
NM_001346898.2:c.2308_2316dup (EGFR)	NP_001333827.1:p.Pro772_His773insAspAsnPro
NM_001346900.2:c.2149_2157dup (EGFR)	NP_001333829.1:p.Pro719_His720insAspAsnPro
NM_001346941.2:c.1507_1515dup (EGFR)	NP_001333870.1:p.Pro505_His506insAspAsnPro
NM_001346899.2:c.2173_2181dup (EGFR)	NP_001333828.1:p.Pro727_His728insAspAsnPro