Canonical Allele Identifier: CA16040590

Gene: EGFR EGFR-AS1

Linked Data

• COSMIC: COSM13007

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181344_55181345delinsTT , CM000669.2:g.55181344_55181345delinsTT	GRCh38
NC_000007.13:g.55249037_55249038delinsTT , CM000669.1:g.55249037_55249038delinsTT	GRCh37
NC_000007.12:g.55216531_55216532delinsTT	NCBI36
NG_007726.3:g.167313_167314delinsTT , LRG_304:g.167313_167314delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2176_2177delinsTT (EGFR)	ENSP00000413354.2:p.Gly726Phe
ENST00000700145.1:c.684_685delinsTT (EGFR)
ENST00000275493.7:c.2335_2336delinsTT (EGFR) MANE Select	ENSP00000275493.2:p.Gly779Phe
ENST00000275493.6:c.2335_2336delinsTT (EGFR)	ENSP00000275493.2:p.Gly779Phe
ENST00000442591.5:c.*28+8416_*28+8417delinsTT (EGFR)	ENSP00000410031.1:n.*28+8416_*28+8417delinsTT
ENST00000454757.6:c.2200_2201delinsTT (EGFR)	ENSP00000395243.3:p.Gly734Phe
ENST00000455089.5:c.2200_2201delinsTT (EGFR)	ENSP00000415559.1:p.Gly734Phe
NM_005228.3:c.2335_2336delinsTT , LRG_304t1:c.2335_2336delinsTT (EGFR)	NP_005219.2:p.Gly779Phe
NR_047551.1:n.1226_1227delinsAA (EGFR-AS1)
NM_001346897.1:c.2200_2201delinsTT (EGFR)	NP_001333826.1:p.Gly734Phe
NM_001346898.1:c.2335_2336delinsTT (EGFR)	NP_001333827.1:p.Gly779Phe
NM_001346899.1:c.2200_2201delinsTT (EGFR)	NP_001333828.1:p.Gly734Phe
NM_001346900.1:c.2176_2177delinsTT (EGFR)	NP_001333829.1:p.Gly726Phe
NM_001346941.1:c.1534_1535delinsTT (EGFR)	NP_001333870.1:p.Gly512Phe
NM_005228.4:c.2335_2336delinsTT (EGFR)	NP_005219.2:p.Gly779Phe
NM_005228.5:c.2335_2336delinsTT (EGFR) MANE Select	NP_005219.2:p.Gly779Phe
NM_001346897.2:c.2200_2201delinsTT (EGFR)	NP_001333826.1:p.Gly734Phe
NM_001346898.2:c.2335_2336delinsTT (EGFR)	NP_001333827.1:p.Gly779Phe
NM_001346900.2:c.2176_2177delinsTT (EGFR)	NP_001333829.1:p.Gly726Phe
NM_001346941.2:c.1534_1535delinsTT (EGFR)	NP_001333870.1:p.Gly512Phe
NM_001346899.2:c.2200_2201delinsTT (EGFR)	NP_001333828.1:p.Gly734Phe