Canonical Allele Identifier: CA2714928733

Gene: EGFR

Linked Data

• dbSNP Id: rs2128964062

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191576del , CM000669.2:g.55191576del	GRCh38
NC_000007.13:g.55259269del , CM000669.1:g.55259269del	GRCh37
NC_000007.12:g.55226763del	NCBI36
NG_007726.3:g.177545del , LRG_304:g.177545del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2311-143del	ENSP00000413354.2:n.2311-143del
ENST00000700145.1:c.819-143del
ENST00000275493.7:c.2470-143del MANE Select	ENSP00000275493.2:n.2470-143del
ENST00000275493.6:c.2470-143del	ENSP00000275493.2:n.2470-143del
ENST00000442591.5:c.*28+18648del	ENSP00000410031.1:n.*28+18648del
ENST00000454757.6:c.2335-143del	ENSP00000395243.3:n.2335-143del
ENST00000455089.5:c.2335-143del	ENSP00000415559.1:n.2335-143del
NM_005228.3:c.2470-143del , LRG_304t1:c.2470-143del	NP_005219.2:n.2470-143del
NM_001346897.1:c.2335-143del	NP_001333826.1:n.2335-143del
NM_001346898.1:c.2470-143del	NP_001333827.1:n.2470-143del
NM_001346899.1:c.2335-143del	NP_001333828.1:n.2335-143del
NM_001346900.1:c.2311-143del	NP_001333829.1:n.2311-143del
NM_001346941.1:c.1669-143del	NP_001333870.1:n.1669-143del
NM_005228.4:c.2470-143del	NP_005219.2:n.2470-143del
NM_005228.5:c.2470-143del MANE Select	NP_005219.2:n.2470-143del
NM_001346897.2:c.2335-143del	NP_001333826.1:n.2335-143del
NM_001346898.2:c.2470-143del	NP_001333827.1:n.2470-143del
NM_001346900.2:c.2311-143del	NP_001333829.1:n.2311-143del
NM_001346941.2:c.1669-143del	NP_001333870.1:n.1669-143del
NM_001346899.2:c.2335-143del	NP_001333828.1:n.2335-143del