Canonical Allele Identifier: CA367577623
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs2128934873

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55154030A>C , CM000669.2:g.55154030A>C GRCh38
NC_000007.13:g.55221723A>C , CM000669.1:g.55221723A>C GRCh37
NC_000007.12:g.55189217A>C NCBI36
NG_007726.3:g.139999A>C , LRG_304:g.139999A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.608A>C ENSP00000413354.2:p.Asp203Ala
ENST00000700144.1:n.957A>C
ENST00000344576.7:c.767A>C ENSP00000345973.2:p.Asp256Ala
ENST00000275493.7:c.767A>C MANE Select ENSP00000275493.2:p.Asp256Ala
ENST00000275493.6:c.767A>C ENSP00000275493.2:p.Asp256Ala
ENST00000342916.7:c.767A>C ENSP00000342376.3:p.Asp256Ala
ENST00000344576.6:c.767A>C ENSP00000345973.2:p.Asp256Ala
ENST00000420316.6:c.767A>C ENSP00000413843.2:p.Asp256Ala
ENST00000442591.5:c.767A>C ENSP00000410031.1:p.Asp256Ala
ENST00000454757.6:c.632A>C ENSP00000395243.3:p.Asp211Ala
ENST00000455089.5:c.632A>C ENSP00000415559.1:p.Asp211Ala
NM_005228.3:c.767A>C , LRG_304t1:c.767A>C NP_005219.2:p.Asp256Ala
NM_201282.1:c.767A>C NP_958439.1:p.Asp256Ala
NM_201283.1:c.767A>C NP_958440.1:p.Asp256Ala
NM_201284.1:c.767A>C NP_958441.1:p.Asp256Ala
NM_001346897.1:c.632A>C NP_001333826.1:p.Asp211Ala
NM_001346898.1:c.767A>C NP_001333827.1:p.Asp256Ala
NM_001346899.1:c.632A>C NP_001333828.1:p.Asp211Ala
NM_001346900.1:c.608A>C NP_001333829.1:p.Asp203Ala
NM_001346941.1:c.89-1800A>C NP_001333870.1:n.89-1800A>C
NM_005228.4:c.767A>C NP_005219.2:p.Asp256Ala
NM_005228.5:c.767A>C MANE Select NP_005219.2:p.Asp256Ala
NM_001346897.2:c.632A>C NP_001333826.1:p.Asp211Ala
NM_001346898.2:c.767A>C NP_001333827.1:p.Asp256Ala
NM_001346900.2:c.608A>C NP_001333829.1:p.Asp203Ala
NM_001346941.2:c.89-1800A>C NP_001333870.1:n.89-1800A>C
NM_201282.2:c.767A>C NP_958439.1:p.Asp256Ala
NM_201284.2:c.767A>C NP_958441.1:p.Asp256Ala
NM_001346899.2:c.632A>C NP_001333828.1:p.Asp211Ala
NM_201283.2:c.767A>C NP_958440.1:p.Asp256Ala