Canonical Allele Identifier: CA367583384

Gene: EGFR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55173927G>T , CM000669.2:g.55173927G>T	GRCh38
NC_000007.13:g.55241620G>T , CM000669.1:g.55241620G>T	GRCh37
NC_000007.12:g.55209114G>T	NCBI36
NG_007726.3:g.159896G>T , LRG_304:g.159896G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.1909G>T	ENSP00000413354.2:p.Glu637Ter
ENST00000700145.1:c.417G>T
ENST00000275493.7:c.2068G>T MANE Select	ENSP00000275493.2:p.Glu690Ter
ENST00000275493.6:c.2068G>T	ENSP00000275493.2:p.Glu690Ter
ENST00000442591.5:c.*28+999G>T	ENSP00000410031.1:n.*28+999G>T
ENST00000454757.6:c.1933G>T	ENSP00000395243.3:p.Glu645Ter
ENST00000455089.5:c.1933G>T	ENSP00000415559.1:p.Glu645Ter
NM_005228.3:c.2068G>T , LRG_304t1:c.2068G>T	NP_005219.2:p.Glu690Ter
NM_001346897.1:c.1933G>T	NP_001333826.1:p.Glu645Ter
NM_001346898.1:c.2068G>T	NP_001333827.1:p.Glu690Ter
NM_001346899.1:c.1933G>T	NP_001333828.1:p.Glu645Ter
NM_001346900.1:c.1909G>T	NP_001333829.1:p.Glu637Ter
NM_001346941.1:c.1267G>T	NP_001333870.1:p.Glu423Ter
NM_005228.4:c.2068G>T	NP_005219.2:p.Glu690Ter
NM_005228.5:c.2068G>T MANE Select	NP_005219.2:p.Glu690Ter
NM_001346897.2:c.1933G>T	NP_001333826.1:p.Glu645Ter
NM_001346898.2:c.2068G>T	NP_001333827.1:p.Glu690Ter
NM_001346900.2:c.1909G>T	NP_001333829.1:p.Glu637Ter
NM_001346941.2:c.1267G>T	NP_001333870.1:p.Glu423Ter
NM_001346899.2:c.1933G>T	NP_001333828.1:p.Glu645Ter