Canonical Allele Identifier: CA367582567

Gene: EGFR

Linked Data

• dbSNP Id: rs1362774341
• MyVariant Identifiers: chr7:g.55268986A>T (hg19) ; chr7:g.55201293A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55201293A>T , CM000669.2:g.55201293A>T	GRCh38
NC_000007.13:g.55268986A>T , CM000669.1:g.55268986A>T	GRCh37
NC_000007.12:g.55236480A>T	NCBI36
NG_007726.3:g.187262A>T , LRG_304:g.187262A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2893A>T	ENSP00000413354.2:p.Ile965Phe
ENST00000700145.1:c.900-4054A>T
ENST00000700146.1:n.796A>T
ENST00000700147.1:n.721A>T
ENST00000275493.7:c.3052A>T MANE Select	ENSP00000275493.2:p.Ile1018Phe
ENST00000275493.6:c.3052A>T	ENSP00000275493.2:p.Ile1018Phe
ENST00000442591.5:c.*28+28365A>T	ENSP00000410031.1:n.*28+28365A>T
ENST00000454757.6:c.2917A>T	ENSP00000395243.3:p.Ile973Phe
ENST00000455089.5:c.2917A>T	ENSP00000415559.1:p.Ile973Phe
NM_005228.3:c.3052A>T , LRG_304t1:c.3052A>T	NP_005219.2:p.Ile1018Phe
NM_001346897.1:c.2917A>T	NP_001333826.1:p.Ile973Phe
NM_001346898.1:c.3052A>T	NP_001333827.1:p.Ile1018Phe
NM_001346899.1:c.2917A>T	NP_001333828.1:p.Ile973Phe
NM_001346900.1:c.2893A>T	NP_001333829.1:p.Ile965Phe
NM_001346941.1:c.2251A>T	NP_001333870.1:p.Ile751Phe
NM_005228.4:c.3052A>T	NP_005219.2:p.Ile1018Phe
NM_005228.5:c.3052A>T MANE Select	NP_005219.2:p.Ile1018Phe
NM_001346897.2:c.2917A>T	NP_001333826.1:p.Ile973Phe
NM_001346898.2:c.3052A>T	NP_001333827.1:p.Ile1018Phe
NM_001346900.2:c.2893A>T	NP_001333829.1:p.Ile965Phe
NM_001346941.2:c.2251A>T	NP_001333870.1:p.Ile751Phe
NM_001346899.2:c.2917A>T	NP_001333828.1:p.Ile973Phe