Canonical Allele Identifier: CA158928351

Gene: EGFR EGFR-AS1

Linked Data

• dbSNP Id: rs121913445
• COSMIC: COSM13554

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181321_55181324delinsGCGTGGACAACCG , CM000669.2:g.55181321_55181324delinsGCGTGGACAACCG	GRCh38
NC_000007.13:g.55249014_55249017delinsGCGTGGACAACCG , CM000669.1:g.55249014_55249017delinsGCGTGGACAACCG	GRCh37
NC_000007.12:g.55216508_55216511delinsGCGTGGACAACCG	NCBI36
NG_007726.3:g.167290_167293delinsGCGTGGACAACCG , LRG_304:g.167290_167293delinsGCGTGGACAACCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2153_2156delinsGCGTGGACAACCG (EGFR)	ENSP00000413354.2:p.Asn718_Pro719delinsSerValAspAsnArg
ENST00000700145.1:c.661_664delinsGCGTGGACAACCG (EGFR)
ENST00000275493.7:c.2312_2315delinsGCGTGGACAACCG (EGFR) MANE Select	ENSP00000275493.2:p.Asn771_Pro772delinsSerValAspAsnArg
ENST00000275493.6:c.2312_2315delinsGCGTGGACAACCG (EGFR)	ENSP00000275493.2:p.Asn771_Pro772delinsSerValAspAsnArg
ENST00000442591.5:c.*28+8393_*28+8396delinsGCGTGGACAACCG (EGFR)	ENSP00000410031.1:n.*28+8393_*28+8396delinsGCGTGGACAACCG
ENST00000454757.6:c.2177_2180delinsGCGTGGACAACCG (EGFR)	ENSP00000395243.3:p.Asn726_Pro727delinsSerValAspAsnArg
ENST00000455089.5:c.2177_2180delinsGCGTGGACAACCG (EGFR)	ENSP00000415559.1:p.Asn726_Pro727delinsSerValAspAsnArg
NM_005228.3:c.2312_2315delinsGCGTGGACAACCG , LRG_304t1:c.2312_2315delinsGCGTGGACAACCG (EGFR)	NP_005219.2:p.Asn771_Pro772delinsSerValAspAsnArg
NR_047551.1:n.1247_1250delinsCGGTTGTCCACGC (EGFR-AS1)
NM_001346897.1:c.2177_2180delinsGCGTGGACAACCG (EGFR)	NP_001333826.1:p.Asn726_Pro727delinsSerValAspAsnArg
NM_001346898.1:c.2312_2315delinsGCGTGGACAACCG (EGFR)	NP_001333827.1:p.Asn771_Pro772delinsSerValAspAsnArg
NM_001346899.1:c.2177_2180delinsGCGTGGACAACCG (EGFR)	NP_001333828.1:p.Asn726_Pro727delinsSerValAspAsnArg
NM_001346900.1:c.2153_2156delinsGCGTGGACAACCG (EGFR)	NP_001333829.1:p.Asn718_Pro719delinsSerValAspAsnArg
NM_001346941.1:c.1511_1514delinsGCGTGGACAACCG (EGFR)	NP_001333870.1:p.Asn504_Pro505delinsSerValAspAsnArg
NM_005228.4:c.2312_2315delinsGCGTGGACAACCG (EGFR)	NP_005219.2:p.Asn771_Pro772delinsSerValAspAsnArg
NM_005228.5:c.2312_2315delinsGCGTGGACAACCG (EGFR) MANE Select	NP_005219.2:p.Asn771_Pro772delinsSerValAspAsnArg
NM_001346897.2:c.2177_2180delinsGCGTGGACAACCG (EGFR)	NP_001333826.1:p.Asn726_Pro727delinsSerValAspAsnArg
NM_001346898.2:c.2312_2315delinsGCGTGGACAACCG (EGFR)	NP_001333827.1:p.Asn771_Pro772delinsSerValAspAsnArg
NM_001346900.2:c.2153_2156delinsGCGTGGACAACCG (EGFR)	NP_001333829.1:p.Asn718_Pro719delinsSerValAspAsnArg
NM_001346941.2:c.1511_1514delinsGCGTGGACAACCG (EGFR)	NP_001333870.1:p.Asn504_Pro505delinsSerValAspAsnArg
NM_001346899.2:c.2177_2180delinsGCGTGGACAACCG (EGFR)	NP_001333828.1:p.Asn726_Pro727delinsSerValAspAsnArg