Canonical Allele Identifier: CA2775498837

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174710_55174716del , CM000669.2:g.55174710_55174716del	GRCh38
NC_000007.13:g.55242403_55242409del , CM000669.1:g.55242403_55242409del	GRCh37
NC_000007.12:g.55209897_55209903del	NCBI36
NG_007726.3:g.160679_160685del , LRG_304:g.160679_160685del

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2026-12_2026-6del	ENSP00000413354.2:n.2026-12_2026-6del
ENST00000700145.1:c.534-12_534-6del
ENST00000275493.7:c.2185-12_2185-6del MANE Select	ENSP00000275493.2:n.2185-12_2185-6del
ENST00000275493.6:c.2185-12_2185-6del	ENSP00000275493.2:n.2185-12_2185-6del
ENST00000442591.5:c.*28+1782_*28+1788del	ENSP00000410031.1:n.*28+1782_*28+1788del
ENST00000454757.6:c.2050-12_2050-6del	ENSP00000395243.3:n.2050-12_2050-6del
ENST00000455089.5:c.2050-12_2050-6del	ENSP00000415559.1:n.2050-12_2050-6del
NM_005228.3:c.2185-12_2185-6del , LRG_304t1:c.2185-12_2185-6del	NP_005219.2:n.2185-12_2185-6del
NM_001346897.1:c.2050-12_2050-6del	NP_001333826.1:n.2050-12_2050-6del
NM_001346898.1:c.2185-12_2185-6del	NP_001333827.1:n.2185-12_2185-6del
NM_001346899.1:c.2050-12_2050-6del	NP_001333828.1:n.2050-12_2050-6del
NM_001346900.1:c.2026-12_2026-6del	NP_001333829.1:n.2026-12_2026-6del
NM_001346941.1:c.1384-12_1384-6del	NP_001333870.1:n.1384-12_1384-6del
NM_005228.4:c.2185-12_2185-6del	NP_005219.2:n.2185-12_2185-6del
NM_005228.5:c.2185-12_2185-6del MANE Select	NP_005219.2:n.2185-12_2185-6del
NM_001346897.2:c.2050-12_2050-6del	NP_001333826.1:n.2050-12_2050-6del
NM_001346898.2:c.2185-12_2185-6del	NP_001333827.1:n.2185-12_2185-6del
NM_001346900.2:c.2026-12_2026-6del	NP_001333829.1:n.2026-12_2026-6del
NM_001346941.2:c.1384-12_1384-6del	NP_001333870.1:n.1384-12_1384-6del
NM_001346899.2:c.2050-12_2050-6del	NP_001333828.1:n.2050-12_2050-6del