Canonical Allele Identifier: CA645561580

Gene: EGFR EGFR-AS1

Linked Data

• dbSNP Id: rs2128958378
• COSMIC: COSM5023008

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181320_55181321insCCA , CM000669.2:g.55181320_55181321insCCA	GRCh38
NC_000007.13:g.55249013_55249014insCCA , CM000669.1:g.55249013_55249014insCCA	GRCh37
NC_000007.12:g.55216507_55216508insCCA	NCBI36
NG_007726.3:g.167289_167290insCCA , LRG_304:g.167289_167290insCCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2152_2153insCCA (EGFR)	ENSP00000413354.2:p.Asp717_Asn718insThr
ENST00000700145.1:c.660_661insCCA (EGFR)
ENST00000275493.7:c.2311_2312insCCA (EGFR) MANE Select	ENSP00000275493.2:p.Asp770_Asn771insThr
ENST00000275493.6:c.2311_2312insCCA (EGFR)	ENSP00000275493.2:p.Asp770_Asn771insThr
ENST00000442591.5:c.*28+8392_*28+8393insCCA (EGFR)	ENSP00000410031.1:n.*28+8392_*28+8393insC...
ENST00000454757.6:c.2176_2177insCCA (EGFR)	ENSP00000395243.3:p.Asp725_Asn726insThr
ENST00000455089.5:c.2176_2177insCCA (EGFR)	ENSP00000415559.1:p.Asp725_Asn726insThr
NM_005228.3:c.2311_2312insCCA , LRG_304t1:c.2311_2312insCCA (EGFR)	NP_005219.2:p.Asp770_Asn771insThr
NR_047551.1:n.1252_1253insGTG (EGFR-AS1)
NM_001346897.1:c.2176_2177insCCA (EGFR)	NP_001333826.1:p.Asp725_Asn726insThr
NM_001346898.1:c.2311_2312insCCA (EGFR)	NP_001333827.1:p.Asp770_Asn771insThr
NM_001346899.1:c.2176_2177insCCA (EGFR)	NP_001333828.1:p.Asp725_Asn726insThr
NM_001346900.1:c.2152_2153insCCA (EGFR)	NP_001333829.1:p.Asp717_Asn718insThr
NM_001346941.1:c.1510_1511insCCA (EGFR)	NP_001333870.1:p.Asp503_Asn504insThr
NM_005228.4:c.2311_2312insCCA (EGFR)	NP_005219.2:p.Asp770_Asn771insThr
NM_005228.5:c.2311_2312insCCA (EGFR) MANE Select	NP_005219.2:p.Asp770_Asn771insThr
NM_001346897.2:c.2176_2177insCCA (EGFR)	NP_001333826.1:p.Asp725_Asn726insThr
NM_001346898.2:c.2311_2312insCCA (EGFR)	NP_001333827.1:p.Asp770_Asn771insThr
NM_001346900.2:c.2152_2153insCCA (EGFR)	NP_001333829.1:p.Asp717_Asn718insThr
NM_001346941.2:c.1510_1511insCCA (EGFR)	NP_001333870.1:p.Asp503_Asn504insThr
NM_001346899.2:c.2176_2177insCCA (EGFR)	NP_001333828.1:p.Asp725_Asn726insThr