Canonical Allele Identifier: CA2682854819

Gene: EGFR

Linked Data

• gnomAD v4: 7-55174602-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174603dup , CM000669.2:g.55174603dup	GRCh38
NC_000007.13:g.55242296dup , CM000669.1:g.55242296dup	GRCh37
NC_000007.12:g.55209790dup	NCBI36
NG_007726.3:g.160572dup , LRG_304:g.160572dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2026-119dup	ENSP00000413354.2:n.2026-119dup
ENST00000700145.1:c.534-119dup
ENST00000275493.7:c.2185-119dup MANE Select	ENSP00000275493.2:n.2185-119dup
ENST00000275493.6:c.2185-119dup	ENSP00000275493.2:n.2185-119dup
ENST00000442591.5:c.*28+1675dup	ENSP00000410031.1:n.*28+1675dup
ENST00000454757.6:c.2050-119dup	ENSP00000395243.3:n.2050-119dup
ENST00000455089.5:c.2050-119dup	ENSP00000415559.1:n.2050-119dup
NM_005228.3:c.2185-119dup , LRG_304t1:c.2185-119dup	NP_005219.2:n.2185-119dup
NM_001346897.1:c.2050-119dup	NP_001333826.1:n.2050-119dup
NM_001346898.1:c.2185-119dup	NP_001333827.1:n.2185-119dup
NM_001346899.1:c.2050-119dup	NP_001333828.1:n.2050-119dup
NM_001346900.1:c.2026-119dup	NP_001333829.1:n.2026-119dup
NM_001346941.1:c.1384-119dup	NP_001333870.1:n.1384-119dup
NM_005228.4:c.2185-119dup	NP_005219.2:n.2185-119dup
NM_005228.5:c.2185-119dup MANE Select	NP_005219.2:n.2185-119dup
NM_001346897.2:c.2050-119dup	NP_001333826.1:n.2050-119dup
NM_001346898.2:c.2185-119dup	NP_001333827.1:n.2185-119dup
NM_001346900.2:c.2026-119dup	NP_001333829.1:n.2026-119dup
NM_001346941.2:c.1384-119dup	NP_001333870.1:n.1384-119dup
NM_001346899.2:c.2050-119dup	NP_001333828.1:n.2050-119dup