Canonical Allele Identifier: CA891842026

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174777_55174796delinsCT , CM000669.2:g.55174777_55174796delinsCT	GRCh38
NC_000007.13:g.55242470_55242489delinsCT , CM000669.1:g.55242470_55242489delinsCT	GRCh37
NC_000007.12:g.55209964_55209983delinsCT	NCBI36
NG_007726.3:g.160746_160765delinsCT , LRG_304:g.160746_160765delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2081_2100delinsCT	ENSP00000413354.2:p.Leu694_Pro700delinsSe...
ENST00000700145.1:c.589_608delinsCT
ENST00000275493.7:c.2240_2259delinsCT MANE Select	ENSP00000275493.2:p.Leu747_Pro753delinsSe...
ENST00000275493.6:c.2240_2259delinsCT	ENSP00000275493.2:p.Leu747_Pro753delinsSe...
ENST00000442591.5:c.*28+1849_*28+1868delinsCT	ENSP00000410031.1:n.*28+1849_*28+1868deli...
ENST00000454757.6:c.2105_2124delinsCT	ENSP00000395243.3:p.Leu702_Pro708delinsSe...
ENST00000455089.5:c.2105_2124delinsCT	ENSP00000415559.1:p.Leu702_Pro708delinsSe...
NM_005228.3:c.2240_2259delinsCT , LRG_304t1:c.2240_2259delinsCT	NP_005219.2:p.Leu747_Pro753delinsSer
NM_001346897.1:c.2105_2124delinsCT	NP_001333826.1:p.Leu702_Pro708delinsSer
NM_001346898.1:c.2240_2259delinsCT	NP_001333827.1:p.Leu747_Pro753delinsSer
NM_001346899.1:c.2105_2124delinsCT	NP_001333828.1:p.Leu702_Pro708delinsSer
NM_001346900.1:c.2081_2100delinsCT	NP_001333829.1:p.Leu694_Pro700delinsSer
NM_001346941.1:c.1439_1458delinsCT	NP_001333870.1:p.Leu480_Pro486delinsSer
NM_005228.4:c.2240_2259delinsCT	NP_005219.2:p.Leu747_Pro753delinsSer
NM_005228.5:c.2240_2259delinsCT MANE Select	NP_005219.2:p.Leu747_Pro753delinsSer
NM_001346897.2:c.2105_2124delinsCT	NP_001333826.1:p.Leu702_Pro708delinsSer
NM_001346898.2:c.2240_2259delinsCT	NP_001333827.1:p.Leu747_Pro753delinsSer
NM_001346900.2:c.2081_2100delinsCT	NP_001333829.1:p.Leu694_Pro700delinsSer
NM_001346941.2:c.1439_1458delinsCT	NP_001333870.1:p.Leu480_Pro486delinsSer
NM_001346899.2:c.2105_2124delinsCT	NP_001333828.1:p.Leu702_Pro708delinsSer