Canonical Allele Identifier: CA1101528455
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs1790782145

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55086707del , CM000669.2:g.55086707del GRCh38
NC_000007.13:g.55154400del , CM000669.1:g.55154400del GRCh37
NC_000007.12:g.55121894del NCBI36
NG_007726.3:g.72676del , LRG_304:g.72676del

Transcript Alleles

HGVS Amino-acid change
ENST00000700144.1:n.279-55579del
ENST00000344576.7:c.89-55579del ENSP00000345973.2:n.89-55579del
ENST00000275493.7:c.89-55579del MANE Select ENSP00000275493.2:n.89-55579del
ENST00000275493.6:c.89-55579del ENSP00000275493.2:n.89-55579del
ENST00000342916.7:c.89-55579del ENSP00000342376.3:n.89-55579del
ENST00000344576.6:c.89-55579del ENSP00000345973.2:n.89-55579del
ENST00000420316.6:c.89-55579del ENSP00000413843.2:n.89-55579del
ENST00000442591.5:c.89-55579del ENSP00000410031.1:n.89-55579del
ENST00000454757.6:c.89-55579del ENSP00000395243.3:n.89-55579del
ENST00000455089.5:c.89-55579del ENSP00000415559.1:n.89-55579del
ENST00000463948.1:n.216-32349del
NM_005228.3:c.89-55579del , LRG_304t1:c.89-55579del NP_005219.2:n.89-55579del
NM_201282.1:c.89-55579del NP_958439.1:n.89-55579del
NM_201283.1:c.89-55579del NP_958440.1:n.89-55579del
NM_201284.1:c.89-55579del NP_958441.1:n.89-55579del
NM_001346897.1:c.89-55579del NP_001333826.1:n.89-55579del
NM_001346898.1:c.89-55579del NP_001333827.1:n.89-55579del
NM_001346899.1:c.89-55579del NP_001333828.1:n.89-55579del
NM_001346941.1:c.88+67342del NP_001333870.1:n.88+67342del
NM_005228.4:c.89-55579del NP_005219.2:n.89-55579del
NM_005228.5:c.89-55579del MANE Select NP_005219.2:n.89-55579del
NM_001346897.2:c.89-55579del NP_001333826.1:n.89-55579del
NM_001346898.2:c.89-55579del NP_001333827.1:n.89-55579del
NM_001346941.2:c.88+67342del NP_001333870.1:n.88+67342del
NM_201282.2:c.89-55579del NP_958439.1:n.89-55579del
NM_201284.2:c.89-55579del NP_958441.1:n.89-55579del
NM_001346899.2:c.89-55579del NP_001333828.1:n.89-55579del
NM_201283.2:c.89-55579del NP_958440.1:n.89-55579del