Canonical Allele Identifier: CA2682854876

Gene: EGFR

Linked Data

• gnomAD v4: 7-55174683-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174685del , CM000669.2:g.55174685del	GRCh38
NC_000007.13:g.55242378del , CM000669.1:g.55242378del	GRCh37
NC_000007.12:g.55209872del	NCBI36
NG_007726.3:g.160654del , LRG_304:g.160654del

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2026-37del	ENSP00000413354.2:n.2026-37del
ENST00000700145.1:c.534-37del
ENST00000275493.7:c.2185-37del MANE Select	ENSP00000275493.2:n.2185-37del
ENST00000275493.6:c.2185-37del	ENSP00000275493.2:n.2185-37del
ENST00000442591.5:c.*28+1757del	ENSP00000410031.1:n.*28+1757del
ENST00000454757.6:c.2050-37del	ENSP00000395243.3:n.2050-37del
ENST00000455089.5:c.2050-37del	ENSP00000415559.1:n.2050-37del
NM_005228.3:c.2185-37del , LRG_304t1:c.2185-37del	NP_005219.2:n.2185-37del
NM_001346897.1:c.2050-37del	NP_001333826.1:n.2050-37del
NM_001346898.1:c.2185-37del	NP_001333827.1:n.2185-37del
NM_001346899.1:c.2050-37del	NP_001333828.1:n.2050-37del
NM_001346900.1:c.2026-37del	NP_001333829.1:n.2026-37del
NM_001346941.1:c.1384-37del	NP_001333870.1:n.1384-37del
NM_005228.4:c.2185-37del	NP_005219.2:n.2185-37del
NM_005228.5:c.2185-37del MANE Select	NP_005219.2:n.2185-37del
NM_001346897.2:c.2050-37del	NP_001333826.1:n.2050-37del
NM_001346898.2:c.2185-37del	NP_001333827.1:n.2185-37del
NM_001346900.2:c.2026-37del	NP_001333829.1:n.2026-37del
NM_001346941.2:c.1384-37del	NP_001333870.1:n.1384-37del
NM_001346899.2:c.2050-37del	NP_001333828.1:n.2050-37del