Canonical Allele Identifier: CA2839978232

Gene: EGFR EGFR-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181345dup , CM000669.2:g.55181345dup	GRCh38
NC_000007.13:g.55249038dup , CM000669.1:g.55249038dup	GRCh37
NC_000007.12:g.55216532dup	NCBI36
NG_007726.3:g.167314dup , LRG_304:g.167314dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2177dup (EGFR)	ENSP00000413354.2:p.Ile727HisfsTer?
ENST00000700145.1:c.685dup (EGFR)
ENST00000275493.7:c.2336dup (EGFR) MANE Select	ENSP00000275493.2:p.Ile780HisfsTer?
ENST00000275493.6:c.2336dup (EGFR)	ENSP00000275493.2:p.Ile780HisfsTer?
ENST00000442591.5:c.*28+8417dup (EGFR)	ENSP00000410031.1:n.*28+8417dup
ENST00000454757.6:c.2201dup (EGFR)	ENSP00000395243.3:p.Ile735HisfsTer?
ENST00000455089.5:c.2201dup (EGFR)	ENSP00000415559.1:p.Ile735HisfsTer?
NM_005228.3:c.2336dup , LRG_304t1:c.2336dup (EGFR)	NP_005219.2:p.Ile780HisfsTer?
NR_047551.1:n.1228dup (EGFR-AS1)
NM_001346897.1:c.2201dup (EGFR)	NP_001333826.1:p.Ile735HisfsTer?
NM_001346898.1:c.2336dup (EGFR)	NP_001333827.1:p.Ile780HisfsTer?
NM_001346899.1:c.2201dup (EGFR)	NP_001333828.1:p.Ile735HisfsTer?
NM_001346900.1:c.2177dup (EGFR)	NP_001333829.1:p.Ile727HisfsTer?
NM_001346941.1:c.1535dup (EGFR)	NP_001333870.1:p.Ile513HisfsTer?
NM_005228.4:c.2336dup (EGFR)	NP_005219.2:p.Ile780HisfsTer?
NM_005228.5:c.2336dup (EGFR) MANE Select	NP_005219.2:p.Ile780HisfsTer?
NM_001346897.2:c.2201dup (EGFR)	NP_001333826.1:p.Ile735HisfsTer?
NM_001346898.2:c.2336dup (EGFR)	NP_001333827.1:p.Ile780HisfsTer?
NM_001346900.2:c.2177dup (EGFR)	NP_001333829.1:p.Ile727HisfsTer?
NM_001346941.2:c.1535dup (EGFR)	NP_001333870.1:p.Ile513HisfsTer?
NM_001346899.2:c.2201dup (EGFR)	NP_001333828.1:p.Ile735HisfsTer?