Canonical Allele Identifier: CA1708922610

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191821_55191822delinsCT , CM000669.2:g.55191821_55191822delinsCT	GRCh38
NC_000007.13:g.55259514_55259515delinsCT , CM000669.1:g.55259514_55259515delinsCT	GRCh37
NC_000007.12:g.55227008_55227009delinsCT	NCBI36
NG_007726.3:g.177790_177791delinsCT , LRG_304:g.177790_177791delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2413_2414delinsCT	ENSP00000413354.2:p.Leu805=
ENST00000700145.1:c.899+22_899+23delinsCT
ENST00000275493.7:c.2572_2573delinsCT MANE Select	ENSP00000275493.2:p.Leu858=
ENST00000275493.6:c.2572_2573delinsCT	ENSP00000275493.2:p.Leu858=
ENST00000442591.5:c.*28+18893_*28+18894delinsCT	ENSP00000410031.1:n.*28+18893_*28+18894delinsCT
ENST00000454757.6:c.2437_2438delinsCT	ENSP00000395243.3:p.Leu813=
ENST00000455089.5:c.2437_2438delinsCT	ENSP00000415559.1:p.Leu813=
NM_005228.3:c.2572_2573delinsCT , LRG_304t1:c.2572_2573delinsCT	NP_005219.2:p.Leu858=
NM_001346897.1:c.2437_2438delinsCT	NP_001333826.1:p.Leu813=
NM_001346898.1:c.2572_2573delinsCT	NP_001333827.1:p.Leu858=
NM_001346899.1:c.2437_2438delinsCT	NP_001333828.1:p.Leu813=
NM_001346900.1:c.2413_2414delinsCT	NP_001333829.1:p.Leu805=
NM_001346941.1:c.1771_1772delinsCT	NP_001333870.1:p.Leu591=
NM_005228.4:c.2572_2573delinsCT	NP_005219.2:p.Leu858=
NM_005228.5:c.2572_2573delinsCT MANE Select	NP_005219.2:p.Leu858=
NM_001346897.2:c.2437_2438delinsCT	NP_001333826.1:p.Leu813=
NM_001346898.2:c.2572_2573delinsCT	NP_001333827.1:p.Leu858=
NM_001346900.2:c.2413_2414delinsCT	NP_001333829.1:p.Leu805=
NM_001346941.2:c.1771_1772delinsCT	NP_001333870.1:p.Leu591=
NM_001346899.2:c.2437_2438delinsCT	NP_001333828.1:p.Leu813=