Canonical Allele Identifier: CA574329403

Gene: EGFR

Linked Data

• dbSNP Id: rs1162848014
• gnomAD v2: 7-55219372-TCTGGTTA-T
• MyVariant Identifiers: chr7:g.55219373_55219379del (hg19) ; chr7:g.55151680_55151686del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55151680_55151686del , CM000669.2:g.55151680_55151686del	GRCh38
NC_000007.13:g.55219373_55219379del , CM000669.1:g.55219373_55219379del	GRCh37
NC_000007.12:g.55186867_55186873del	NCBI36
NG_007726.3:g.137649_137655del , LRG_304:g.137649_137655del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.469+318_469+324del	ENSP00000413354.2:n.469+318_469+324del
ENST00000700144.1:n.818+318_818+324del
ENST00000344576.7:c.628+318_628+324del	ENSP00000345973.2:n.628+318_628+324del
ENST00000275493.7:c.628+318_628+324del MANE Select	ENSP00000275493.2:n.628+318_628+324del
ENST00000275493.6:c.628+318_628+324del	ENSP00000275493.2:n.628+318_628+324del
ENST00000342916.7:c.628+318_628+324del	ENSP00000342376.3:n.628+318_628+324del
ENST00000344576.6:c.628+318_628+324del	ENSP00000345973.2:n.628+318_628+324del
ENST00000420316.6:c.628+318_628+324del	ENSP00000413843.2:n.628+318_628+324del
ENST00000442591.5:c.628+318_628+324del	ENSP00000410031.1:n.628+318_628+324del
ENST00000454757.6:c.493+318_493+324del	ENSP00000395243.3:n.493+318_493+324del
ENST00000455089.5:c.493+318_493+324del	ENSP00000415559.1:n.493+318_493+324del
NM_005228.3:c.628+318_628+324del , LRG_304t1:c.628+318_628+324del	NP_005219.2:n.628+318_628+324del
NM_201282.1:c.628+318_628+324del	NP_958439.1:n.628+318_628+324del
NM_201283.1:c.628+318_628+324del	NP_958440.1:n.628+318_628+324del
NM_201284.1:c.628+318_628+324del	NP_958441.1:n.628+318_628+324del
NM_001346897.1:c.493+318_493+324del	NP_001333826.1:n.493+318_493+324del
NM_001346898.1:c.628+318_628+324del	NP_001333827.1:n.628+318_628+324del
NM_001346899.1:c.493+318_493+324del	NP_001333828.1:n.493+318_493+324del
NM_001346900.1:c.469+318_469+324del	NP_001333829.1:n.469+318_469+324del
NM_001346941.1:c.89-4150_89-4144del	NP_001333870.1:n.89-4150_89-4144del
NM_005228.4:c.628+318_628+324del	NP_005219.2:n.628+318_628+324del
NM_005228.5:c.628+318_628+324del MANE Select	NP_005219.2:n.628+318_628+324del
NM_001346897.2:c.493+318_493+324del	NP_001333826.1:n.493+318_493+324del
NM_001346898.2:c.628+318_628+324del	NP_001333827.1:n.628+318_628+324del
NM_001346900.2:c.469+318_469+324del	NP_001333829.1:n.469+318_469+324del
NM_001346941.2:c.89-4150_89-4144del	NP_001333870.1:n.89-4150_89-4144del
NM_201282.2:c.628+318_628+324del	NP_958439.1:n.628+318_628+324del
NM_201284.2:c.628+318_628+324del	NP_958441.1:n.628+318_628+324del
NM_001346899.2:c.493+318_493+324del	NP_001333828.1:n.493+318_493+324del
NM_201283.2:c.628+318_628+324del	NP_958440.1:n.628+318_628+324del