Canonical Allele Identifier: CA367580853

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55165352G>A , CM000669.2:g.55165352G>A	GRCh38
NC_000007.13:g.55233045G>A , CM000669.1:g.55233045G>A	GRCh37
NC_000007.12:g.55200539G>A	NCBI36
NG_007726.3:g.151321G>A , LRG_304:g.151321G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.1636G>A	ENSP00000413354.2:p.Val546Ile
ENST00000700145.1:c.144G>A
ENST00000344576.7:c.1795G>A	ENSP00000345973.2:p.Val599Ile
ENST00000275493.7:c.1795G>A MANE Select	ENSP00000275493.2:p.Val599Ile
ENST00000275493.6:c.1795G>A	ENSP00000275493.2:p.Val599Ile
ENST00000342916.7:c.1795G>A	ENSP00000342376.3:p.Val599Ile
ENST00000344576.6:c.1795G>A	ENSP00000345973.2:p.Val599Ile
ENST00000442591.5:c.1795G>A	ENSP00000410031.1:p.Val599Ile
ENST00000454757.6:c.1660G>A	ENSP00000395243.3:p.Val554Ile
ENST00000455089.5:c.1660G>A	ENSP00000415559.1:p.Val554Ile
NM_005228.3:c.1795G>A , LRG_304t1:c.1795G>A	NP_005219.2:p.Val599Ile
NM_201282.1:c.1795G>A	NP_958439.1:p.Val599Ile
NM_201284.1:c.1795G>A	NP_958441.1:p.Val599Ile
NM_001346897.1:c.1660G>A	NP_001333826.1:p.Val554Ile
NM_001346898.1:c.1795G>A	NP_001333827.1:p.Val599Ile
NM_001346899.1:c.1660G>A	NP_001333828.1:p.Val554Ile
NM_001346900.1:c.1636G>A	NP_001333829.1:p.Val546Ile
NM_001346941.1:c.994G>A	NP_001333870.1:p.Val332Ile
NM_005228.4:c.1795G>A	NP_005219.2:p.Val599Ile
NM_005228.5:c.1795G>A MANE Select	NP_005219.2:p.Val599Ile
NM_001346897.2:c.1660G>A	NP_001333826.1:p.Val554Ile
NM_001346898.2:c.1795G>A	NP_001333827.1:p.Val599Ile
NM_001346900.2:c.1636G>A	NP_001333829.1:p.Val546Ile
NM_001346941.2:c.994G>A	NP_001333870.1:p.Val332Ile
NM_201282.2:c.1795G>A	NP_958439.1:p.Val599Ile
NM_201284.2:c.1795G>A	NP_958441.1:p.Val599Ile
NM_001346899.2:c.1660G>A	NP_001333828.1:p.Val554Ile