Canonical Allele Identifier: CA839809391
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs1383549762

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55168345del , CM000669.2:g.55168345del GRCh38
NC_000007.13:g.55236038del , CM000669.1:g.55236038del GRCh37
NC_000007.12:g.55203532del NCBI36
NG_007726.3:g.154314del , LRG_304:g.154314del

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.1722-2830del ENSP00000413354.2:n.1722-2830del
ENST00000700145.1:c.230-2830del
ENST00000344576.7:c.1881-1962del ENSP00000345973.2:n.1881-1962del
ENST00000275493.7:c.1881-2830del MANE Select ENSP00000275493.2:n.1881-2830del
ENST00000275493.6:c.1881-2830del ENSP00000275493.2:n.1881-2830del
ENST00000342916.7:c.1881-178del ENSP00000342376.3:n.1881-178del
ENST00000344576.6:c.1881-1962del ENSP00000345973.2:n.1881-1962del
ENST00000442591.5:c.1881-2830del ENSP00000410031.1:n.1881-2830del
ENST00000454757.6:c.1746-2830del ENSP00000395243.3:n.1746-2830del
ENST00000455089.5:c.1746-2830del ENSP00000415559.1:n.1746-2830del
NM_005228.3:c.1881-2830del , LRG_304t1:c.1881-2830del NP_005219.2:n.1881-2830del
NM_201282.1:c.1881-178del NP_958439.1:n.1881-178del
NM_201284.1:c.1881-1962del NP_958441.1:n.1881-1962del
NM_001346897.1:c.1746-2830del NP_001333826.1:n.1746-2830del
NM_001346898.1:c.1881-2830del NP_001333827.1:n.1881-2830del
NM_001346899.1:c.1746-2830del NP_001333828.1:n.1746-2830del
NM_001346900.1:c.1722-2830del NP_001333829.1:n.1722-2830del
NM_001346941.1:c.1080-2830del NP_001333870.1:n.1080-2830del
NM_005228.4:c.1881-2830del NP_005219.2:n.1881-2830del
NM_005228.5:c.1881-2830del MANE Select NP_005219.2:n.1881-2830del
NM_001346897.2:c.1746-2830del NP_001333826.1:n.1746-2830del
NM_001346898.2:c.1881-2830del NP_001333827.1:n.1881-2830del
NM_001346900.2:c.1722-2830del NP_001333829.1:n.1722-2830del
NM_001346941.2:c.1080-2830del NP_001333870.1:n.1080-2830del
NM_201282.2:c.1881-178del NP_958439.1:n.1881-178del
NM_201284.2:c.1881-1962del NP_958441.1:n.1881-1962del
NM_001346899.2:c.1746-2830del NP_001333828.1:n.1746-2830del