Canonical Allele Identifier: CA645561589

Gene: EGFR EGFR-AS1

Linked Data

• dbSNP Id: rs2128958391
• COSMIC: COSM53189

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181320delinsGGTT , CM000669.2:g.55181320delinsGGTT	GRCh38
NC_000007.13:g.55249013delinsGGTT , CM000669.1:g.55249013delinsGGTT	GRCh37
NC_000007.12:g.55216507delinsGGTT	NCBI36
NG_007726.3:g.167289delinsGGTT , LRG_304:g.167289delinsGGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2152delinsGGTT (EGFR)	ENSP00000413354.2:p.Asn718delinsGlyTyr
ENST00000700145.1:c.660delinsGGTT (EGFR)
ENST00000275493.7:c.2311delinsGGTT (EGFR) MANE Select	ENSP00000275493.2:p.Asn771delinsGlyTyr
ENST00000275493.6:c.2311delinsGGTT (EGFR)	ENSP00000275493.2:p.Asn771delinsGlyTyr
ENST00000442591.5:c.*28+8392delinsGGTT (EGFR)	ENSP00000410031.1:n.*28+8392delinsGGTT
ENST00000454757.6:c.2176delinsGGTT (EGFR)	ENSP00000395243.3:p.Asn726delinsGlyTyr
ENST00000455089.5:c.2176delinsGGTT (EGFR)	ENSP00000415559.1:p.Asn726delinsGlyTyr
NM_005228.3:c.2311delinsGGTT , LRG_304t1:c.2311delinsGGTT (EGFR)	NP_005219.2:p.Asn771delinsGlyTyr
NR_047551.1:n.1251delinsAACC (EGFR-AS1)
NM_001346897.1:c.2176delinsGGTT (EGFR)	NP_001333826.1:p.Asn726delinsGlyTyr
NM_001346898.1:c.2311delinsGGTT (EGFR)	NP_001333827.1:p.Asn771delinsGlyTyr
NM_001346899.1:c.2176delinsGGTT (EGFR)	NP_001333828.1:p.Asn726delinsGlyTyr
NM_001346900.1:c.2152delinsGGTT (EGFR)	NP_001333829.1:p.Asn718delinsGlyTyr
NM_001346941.1:c.1510delinsGGTT (EGFR)	NP_001333870.1:p.Asn504delinsGlyTyr
NM_005228.4:c.2311delinsGGTT (EGFR)	NP_005219.2:p.Asn771delinsGlyTyr
NM_005228.5:c.2311delinsGGTT (EGFR) MANE Select	NP_005219.2:p.Asn771delinsGlyTyr
NM_001346897.2:c.2176delinsGGTT (EGFR)	NP_001333826.1:p.Asn726delinsGlyTyr
NM_001346898.2:c.2311delinsGGTT (EGFR)	NP_001333827.1:p.Asn771delinsGlyTyr
NM_001346900.2:c.2152delinsGGTT (EGFR)	NP_001333829.1:p.Asn718delinsGlyTyr
NM_001346941.2:c.1510delinsGGTT (EGFR)	NP_001333870.1:p.Asn504delinsGlyTyr
NM_001346899.2:c.2176delinsGGTT (EGFR)	NP_001333828.1:p.Asn726delinsGlyTyr