Canonical Allele Identifier: CA367580079
Gene: EGFR HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.2477A>C MANE Select ENSP00000275493.2:p.Asn826Thr
ENST00000275493.6:c.2477A>C ENSP00000275493.2:p.Asn826Thr
ENST00000442591.5:c.*28+18798A>C ENSP00000410031.1:n.*28+18798A>C
ENST00000454757.6:c.2342A>C ENSP00000395243.3:p.Asn781Thr
ENST00000455089.5:c.2342A>C ENSP00000415559.1:p.Asn781Thr
NM_005228.3:c.2477A>C , LRG_304t1:c.2477A>C NP_005219.2:p.Asn826Thr
NM_001346897.1:c.2342A>C NP_001333826.1:p.Asn781Thr
NM_001346898.1:c.2477A>C NP_001333827.1:p.Asn826Thr
NM_001346899.1:c.2342A>C NP_001333828.1:p.Asn781Thr
NM_001346900.1:c.2318A>C NP_001333829.1:p.Asn773Thr
NM_001346941.1:c.1676A>C NP_001333870.1:p.Asn559Thr
NM_005228.4:c.2477A>C NP_005219.2:p.Asn826Thr
NM_005228.5:c.2477A>C MANE Select NP_005219.2:p.Asn826Thr
NM_001346897.2:c.2342A>C NP_001333826.1:p.Asn781Thr
NM_001346898.2:c.2477A>C NP_001333827.1:p.Asn826Thr
NM_001346900.2:c.2318A>C NP_001333829.1:p.Asn773Thr
NM_001346941.2:c.1676A>C NP_001333870.1:p.Asn559Thr
NM_001346899.2:c.2342A>C NP_001333828.1:p.Asn781Thr