Canonical Allele Identifier: CA367580315

Gene: EGFR

Linked Data

• dbSNP Id: rs2128964676
• MyVariant Identifiers: chr7:g.55259537A>T (hg19) ; chr7:g.55191844A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191844A>T , CM000669.2:g.55191844A>T	GRCh38
NC_000007.13:g.55259537A>T , CM000669.1:g.55259537A>T	GRCh37
NC_000007.12:g.55227031A>T	NCBI36
NG_007726.3:g.177813A>T , LRG_304:g.177813A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2436A>T	ENSP00000413354.2:p.Glu812Asp
ENST00000700145.1:c.899+45A>T
ENST00000275493.7:c.2595A>T MANE Select	ENSP00000275493.2:p.Glu865Asp
ENST00000275493.6:c.2595A>T	ENSP00000275493.2:p.Glu865Asp
ENST00000442591.5:c.*28+18916A>T	ENSP00000410031.1:n.*28+18916A>T
ENST00000454757.6:c.2460A>T	ENSP00000395243.3:p.Glu820Asp
ENST00000455089.5:c.2460A>T	ENSP00000415559.1:p.Glu820Asp
NM_005228.3:c.2595A>T , LRG_304t1:c.2595A>T	NP_005219.2:p.Glu865Asp
NM_001346897.1:c.2460A>T	NP_001333826.1:p.Glu820Asp
NM_001346898.1:c.2595A>T	NP_001333827.1:p.Glu865Asp
NM_001346899.1:c.2460A>T	NP_001333828.1:p.Glu820Asp
NM_001346900.1:c.2436A>T	NP_001333829.1:p.Glu812Asp
NM_001346941.1:c.1794A>T	NP_001333870.1:p.Glu598Asp
NM_005228.4:c.2595A>T	NP_005219.2:p.Glu865Asp
NM_005228.5:c.2595A>T MANE Select	NP_005219.2:p.Glu865Asp
NM_001346897.2:c.2460A>T	NP_001333826.1:p.Glu820Asp
NM_001346898.2:c.2595A>T	NP_001333827.1:p.Glu865Asp
NM_001346900.2:c.2436A>T	NP_001333829.1:p.Glu812Asp
NM_001346941.2:c.1794A>T	NP_001333870.1:p.Glu598Asp
NM_001346899.2:c.2460A>T	NP_001333828.1:p.Glu820Asp