Canonical Allele Identifier: CA2682854829

Gene: EGFR

Linked Data

• gnomAD v4: 7-55174613-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174616del , CM000669.2:g.55174616del	GRCh38
NC_000007.13:g.55242309del , CM000669.1:g.55242309del	GRCh37
NC_000007.12:g.55209803del	NCBI36
NG_007726.3:g.160585del , LRG_304:g.160585del

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2026-106del	ENSP00000413354.2:n.2026-106del
ENST00000700145.1:c.534-106del
ENST00000275493.7:c.2185-106del MANE Select	ENSP00000275493.2:n.2185-106del
ENST00000275493.6:c.2185-106del	ENSP00000275493.2:n.2185-106del
ENST00000442591.5:c.*28+1688del	ENSP00000410031.1:n.*28+1688del
ENST00000454757.6:c.2050-106del	ENSP00000395243.3:n.2050-106del
ENST00000455089.5:c.2050-106del	ENSP00000415559.1:n.2050-106del
NM_005228.3:c.2185-106del , LRG_304t1:c.2185-106del	NP_005219.2:n.2185-106del
NM_001346897.1:c.2050-106del	NP_001333826.1:n.2050-106del
NM_001346898.1:c.2185-106del	NP_001333827.1:n.2185-106del
NM_001346899.1:c.2050-106del	NP_001333828.1:n.2050-106del
NM_001346900.1:c.2026-106del	NP_001333829.1:n.2026-106del
NM_001346941.1:c.1384-106del	NP_001333870.1:n.1384-106del
NM_005228.4:c.2185-106del	NP_005219.2:n.2185-106del
NM_005228.5:c.2185-106del MANE Select	NP_005219.2:n.2185-106del
NM_001346897.2:c.2050-106del	NP_001333826.1:n.2050-106del
NM_001346898.2:c.2185-106del	NP_001333827.1:n.2185-106del
NM_001346900.2:c.2026-106del	NP_001333829.1:n.2026-106del
NM_001346941.2:c.1384-106del	NP_001333870.1:n.1384-106del
NM_001346899.2:c.2050-106del	NP_001333828.1:n.2050-106del