Canonical Allele Identifier: CA367580077
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs2128964363
COSMIC: COSM13193

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55191726A>G , CM000669.2:g.55191726A>G GRCh38
NC_000007.13:g.55259419A>G , CM000669.1:g.55259419A>G GRCh37
NC_000007.12:g.55226913A>G NCBI36
NG_007726.3:g.177695A>G , LRG_304:g.177695A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2318A>G ENSP00000413354.2:p.Asn773Ser
ENST00000700145.1:c.826A>G
ENST00000275493.7:c.2477A>G MANE Select ENSP00000275493.2:p.Asn826Ser
ENST00000275493.6:c.2477A>G ENSP00000275493.2:p.Asn826Ser
ENST00000442591.5:c.*28+18798A>G ENSP00000410031.1:n.*28+18798A>G
ENST00000454757.6:c.2342A>G ENSP00000395243.3:p.Asn781Ser
ENST00000455089.5:c.2342A>G ENSP00000415559.1:p.Asn781Ser
NM_005228.3:c.2477A>G , LRG_304t1:c.2477A>G NP_005219.2:p.Asn826Ser
NM_001346897.1:c.2342A>G NP_001333826.1:p.Asn781Ser
NM_001346898.1:c.2477A>G NP_001333827.1:p.Asn826Ser
NM_001346899.1:c.2342A>G NP_001333828.1:p.Asn781Ser
NM_001346900.1:c.2318A>G NP_001333829.1:p.Asn773Ser
NM_001346941.1:c.1676A>G NP_001333870.1:p.Asn559Ser
NM_005228.4:c.2477A>G NP_005219.2:p.Asn826Ser
NM_005228.5:c.2477A>G MANE Select NP_005219.2:p.Asn826Ser
NM_001346897.2:c.2342A>G NP_001333826.1:p.Asn781Ser
NM_001346898.2:c.2477A>G NP_001333827.1:p.Asn826Ser
NM_001346900.2:c.2318A>G NP_001333829.1:p.Asn773Ser
NM_001346941.2:c.1676A>G NP_001333870.1:p.Asn559Ser
NM_001346899.2:c.2342A>G NP_001333828.1:p.Asn781Ser