Canonical Allele Identifier: CA367584223

Gene: EGFR

Linked Data

• MyVariant Identifiers: chr7:g.55242503A>T (hg19) ; chr7:g.55174810A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174810A>T , CM000669.2:g.55174810A>T	GRCh38
NC_000007.13:g.55242503A>T , CM000669.1:g.55242503A>T	GRCh37
NC_000007.12:g.55209997A>T	NCBI36
NG_007726.3:g.160779A>T , LRG_304:g.160779A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2114A>T	ENSP00000413354.2:p.Glu705Val
ENST00000700145.1:c.622A>T
ENST00000275493.7:c.2273A>T MANE Select	ENSP00000275493.2:p.Glu758Val
ENST00000275493.6:c.2273A>T	ENSP00000275493.2:p.Glu758Val
ENST00000442591.5:c.*28+1882A>T	ENSP00000410031.1:n.*28+1882A>T
ENST00000454757.6:c.2138A>T	ENSP00000395243.3:p.Glu713Val
ENST00000455089.5:c.2138A>T	ENSP00000415559.1:p.Glu713Val
NM_005228.3:c.2273A>T , LRG_304t1:c.2273A>T	NP_005219.2:p.Glu758Val
NM_001346897.1:c.2138A>T	NP_001333826.1:p.Glu713Val
NM_001346898.1:c.2273A>T	NP_001333827.1:p.Glu758Val
NM_001346899.1:c.2138A>T	NP_001333828.1:p.Glu713Val
NM_001346900.1:c.2114A>T	NP_001333829.1:p.Glu705Val
NM_001346941.1:c.1472A>T	NP_001333870.1:p.Glu491Val
NM_005228.4:c.2273A>T	NP_005219.2:p.Glu758Val
NM_005228.5:c.2273A>T MANE Select	NP_005219.2:p.Glu758Val
NM_001346897.2:c.2138A>T	NP_001333826.1:p.Glu713Val
NM_001346898.2:c.2273A>T	NP_001333827.1:p.Glu758Val
NM_001346900.2:c.2114A>T	NP_001333829.1:p.Glu705Val
NM_001346941.2:c.1472A>T	NP_001333870.1:p.Glu491Val
NM_001346899.2:c.2138A>T	NP_001333828.1:p.Glu713Val