Canonical Allele Identifier: CA2578893463

Gene: EGFR

Linked Data

• dbSNP Id: rs2128964140

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191620del , CM000669.2:g.55191620del	GRCh38
NC_000007.13:g.55259313del , CM000669.1:g.55259313del	GRCh37
NC_000007.12:g.55226807del	NCBI36
NG_007726.3:g.177589del , LRG_304:g.177589del

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2311-99del	ENSP00000413354.2:n.2311-99del
ENST00000700145.1:c.819-99del
ENST00000275493.7:c.2470-99del MANE Select	ENSP00000275493.2:n.2470-99del
ENST00000275493.6:c.2470-99del	ENSP00000275493.2:n.2470-99del
ENST00000442591.5:c.*28+18692del	ENSP00000410031.1:n.*28+18692del
ENST00000454757.6:c.2335-99del	ENSP00000395243.3:n.2335-99del
ENST00000455089.5:c.2335-99del	ENSP00000415559.1:n.2335-99del
NM_005228.3:c.2470-99del , LRG_304t1:c.2470-99del	NP_005219.2:n.2470-99del
NM_001346897.1:c.2335-99del	NP_001333826.1:n.2335-99del
NM_001346898.1:c.2470-99del	NP_001333827.1:n.2470-99del
NM_001346899.1:c.2335-99del	NP_001333828.1:n.2335-99del
NM_001346900.1:c.2311-99del	NP_001333829.1:n.2311-99del
NM_001346941.1:c.1669-99del	NP_001333870.1:n.1669-99del
NM_005228.4:c.2470-99del	NP_005219.2:n.2470-99del
NM_005228.5:c.2470-99del MANE Select	NP_005219.2:n.2470-99del
NM_001346897.2:c.2335-99del	NP_001333826.1:n.2335-99del
NM_001346898.2:c.2470-99del	NP_001333827.1:n.2470-99del
NM_001346900.2:c.2311-99del	NP_001333829.1:n.2311-99del
NM_001346941.2:c.1669-99del	NP_001333870.1:n.1669-99del
NM_001346899.2:c.2335-99del	NP_001333828.1:n.2335-99del