Canonical Allele Identifier: CA158940457

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55205304A>G , CM000669.2:g.55205304A>G	GRCh38
NC_000007.13:g.55272997A>G , CM000669.1:g.55272997A>G	GRCh37
NC_000007.12:g.55240491A>G	NCBI36
NG_007726.3:g.191273A>G , LRG_304:g.191273A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005228.5:c.3320A>G MANE Select	NP_005219.2:p.Asn1107Ser
ENST00000275493.7:c.3320A>G MANE Select	ENSP00000275493.2:p.Asn1107Ser
NM_001346899.1:c.3185A>G	NP_001333828.1:p.Asn1062Ser
NM_001346899.2:c.3185A>G	NP_001333828.1:p.Asn1062Ser
NM_001346900.1:c.3161A>G	NP_001333829.1:p.Asn1054Ser
NM_001346900.2:c.3161A>G	NP_001333829.1:p.Asn1054Ser
NM_001346941.1:c.2519A>G	NP_001333870.1:p.Asn840Ser
NM_001346941.2:c.2519A>G	NP_001333870.1:p.Asn840Ser
NM_005228.3:c.3320A>G , LRG_304t1:c.3320A>G	NP_005219.2:p.Asn1107Ser
NM_005228.4:c.3320A>G	NP_005219.2:p.Asn1107Ser
ENST00000275493.6:c.3320A>G	ENSP00000275493.2:p.Asn1107Ser
ENST00000442591.5:c.*28+32376A>G	ENSP00000410031.1:n.*28+32376A>G
ENST00000450046.2:c.3161A>G	ENSP00000413354.2:p.Asn1054Ser
ENST00000454757.6:c.3185A>G	ENSP00000395243.3:p.Asn1062Ser
ENST00000700145.1:c.900-43A>G
ENST00000700146.1:n.1064A>G
ENST00000700147.1:n.989A>G