Canonical Allele Identifier: CA2580077235

Gene: EGFR

Linked Data

• ClinVar Variation Id: 2003462
• ClinVar RCV Id: RCV002811197

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55151364dup , CM000669.2:g.55151364dup	GRCh38
NC_000007.13:g.55219057dup , CM000669.1:g.55219057dup	GRCh37
NC_000007.12:g.55186551dup	NCBI36
NG_007726.3:g.137333dup , LRG_304:g.137333dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.469+2dup	ENSP00000413354.2:n.469+2dup
ENST00000700144.1:n.818+2dup
ENST00000344576.7:c.628+2dup	ENSP00000345973.2:n.628+2dup
ENST00000275493.7:c.628+2dup MANE Select	ENSP00000275493.2:n.628+2dup
ENST00000275493.6:c.628+2dup	ENSP00000275493.2:n.628+2dup
ENST00000342916.7:c.628+2dup	ENSP00000342376.3:n.628+2dup
ENST00000344576.6:c.628+2dup	ENSP00000345973.2:n.628+2dup
ENST00000420316.6:c.628+2dup	ENSP00000413843.2:n.628+2dup
ENST00000442591.5:c.628+2dup	ENSP00000410031.1:n.628+2dup
ENST00000454757.6:c.493+2dup	ENSP00000395243.3:n.493+2dup
ENST00000455089.5:c.493+2dup	ENSP00000415559.1:n.493+2dup
NM_005228.3:c.628+2dup , LRG_304t1:c.628+2dup	NP_005219.2:n.628+2dup
NM_201282.1:c.628+2dup	NP_958439.1:n.628+2dup
NM_201283.1:c.628+2dup	NP_958440.1:n.628+2dup
NM_201284.1:c.628+2dup	NP_958441.1:n.628+2dup
NM_001346897.1:c.493+2dup	NP_001333826.1:n.493+2dup
NM_001346898.1:c.628+2dup	NP_001333827.1:n.628+2dup
NM_001346899.1:c.493+2dup	NP_001333828.1:n.493+2dup
NM_001346900.1:c.469+2dup	NP_001333829.1:n.469+2dup
NM_001346941.1:c.89-4466dup	NP_001333870.1:n.89-4466dup
NM_005228.4:c.628+2dup	NP_005219.2:n.628+2dup
NM_005228.5:c.628+2dup MANE Select	NP_005219.2:n.628+2dup
NM_001346897.2:c.493+2dup	NP_001333826.1:n.493+2dup
NM_001346898.2:c.628+2dup	NP_001333827.1:n.628+2dup
NM_001346900.2:c.469+2dup	NP_001333829.1:n.469+2dup
NM_001346941.2:c.89-4466dup	NP_001333870.1:n.89-4466dup
NM_201282.2:c.628+2dup	NP_958439.1:n.628+2dup
NM_201284.2:c.628+2dup	NP_958441.1:n.628+2dup
NM_001346899.2:c.493+2dup	NP_001333828.1:n.493+2dup
NM_201283.2:c.628+2dup	NP_958440.1:n.628+2dup