Canonical Allele Identifier: CA645561584

Gene: EGFR EGFR-AS1

Linked Data

• dbSNP Id: rs2128958374
• COSMIC: COSM13004

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181319_55181320insGGC , CM000669.2:g.55181319_55181320insGGC	GRCh38
NC_000007.13:g.55249012_55249013insGGC , CM000669.1:g.55249012_55249013insGGC	GRCh37
NC_000007.12:g.55216506_55216507insGGC	NCBI36
NG_007726.3:g.167288_167289insGGC , LRG_304:g.167288_167289insGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2151_2152insGGC (EGFR)	ENSP00000413354.2:p.Asp717_Asn718insGly
ENST00000700145.1:c.659_660insGGC (EGFR)
ENST00000275493.7:c.2310_2311insGGC (EGFR) MANE Select	ENSP00000275493.2:p.Asp770_Asn771insGly
ENST00000275493.6:c.2310_2311insGGC (EGFR)	ENSP00000275493.2:p.Asp770_Asn771insGly
ENST00000442591.5:c.*28+8391_*28+8392insGGC (EGFR)	ENSP00000410031.1:n.*28+8391_*28+8392insGGC
ENST00000454757.6:c.2175_2176insGGC (EGFR)	ENSP00000395243.3:p.Asp725_Asn726insGly
ENST00000455089.5:c.2175_2176insGGC (EGFR)	ENSP00000415559.1:p.Asp725_Asn726insGly
NM_005228.3:c.2310_2311insGGC , LRG_304t1:c.2310_2311insGGC (EGFR)	NP_005219.2:p.Asp770_Asn771insGly
NR_047551.1:n.1252_1253insCCG (EGFR-AS1)
NM_001346897.1:c.2175_2176insGGC (EGFR)	NP_001333826.1:p.Asp725_Asn726insGly
NM_001346898.1:c.2310_2311insGGC (EGFR)	NP_001333827.1:p.Asp770_Asn771insGly
NM_001346899.1:c.2175_2176insGGC (EGFR)	NP_001333828.1:p.Asp725_Asn726insGly
NM_001346900.1:c.2151_2152insGGC (EGFR)	NP_001333829.1:p.Asp717_Asn718insGly
NM_001346941.1:c.1509_1510insGGC (EGFR)	NP_001333870.1:p.Asp503_Asn504insGly
NM_005228.4:c.2310_2311insGGC (EGFR)	NP_005219.2:p.Asp770_Asn771insGly
NM_005228.5:c.2310_2311insGGC (EGFR) MANE Select	NP_005219.2:p.Asp770_Asn771insGly
NM_001346897.2:c.2175_2176insGGC (EGFR)	NP_001333826.1:p.Asp725_Asn726insGly
NM_001346898.2:c.2310_2311insGGC (EGFR)	NP_001333827.1:p.Asp770_Asn771insGly
NM_001346900.2:c.2151_2152insGGC (EGFR)	NP_001333829.1:p.Asp717_Asn718insGly
NM_001346941.2:c.1509_1510insGGC (EGFR)	NP_001333870.1:p.Asp503_Asn504insGly
NM_001346899.2:c.2175_2176insGGC (EGFR)	NP_001333828.1:p.Asp725_Asn726insGly