Canonical Allele Identifier: CA135857
Gene: EGFR HGNC NCBI
EGFR-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55181321_55181323dup , CM000669.2:g.55181321_55181323dup GRCh38
NC_000007.13:g.55249014_55249016dup , CM000669.1:g.55249014_55249016dup GRCh37
NC_000007.12:g.55216508_55216510dup NCBI36
NG_007726.3:g.167290_167292dup , LRG_304:g.167290_167292dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000450046.2:c.2153_2155dup (EGFR) ENSP00000413354.2:p.Asn718_Pro719insHis
ENST00000700145.1:c.661_663dup (EGFR)
ENST00000275493.7:c.2312_2314dup (EGFR) MANE Select ENSP00000275493.2:p.Asn771_Pro772insHis
ENST00000275493.6:c.2312_2314dup (EGFR) ENSP00000275493.2:p.Asn771_Pro772insHis
ENST00000442591.5:c.*28+8393_*28+8395dup (EGFR) ENSP00000410031.1:n.*28+8393_*28+8395dup
ENST00000454757.6:c.2177_2179dup (EGFR) ENSP00000395243.3:p.Asn726_Pro727insHis
ENST00000455089.5:c.2177_2179dup (EGFR) ENSP00000415559.1:p.Asn726_Pro727insHis
NM_005228.3:c.2312_2314dup , LRG_304t1:c.2312_2314dup (EGFR) NP_005219.2:p.Asn771_Pro772insHis
NR_047551.1:n.1248_1250dup (EGFR-AS1)
NM_001346897.1:c.2177_2179dup (EGFR) NP_001333826.1:p.Asn726_Pro727insHis
NM_001346898.1:c.2312_2314dup (EGFR) NP_001333827.1:p.Asn771_Pro772insHis
NM_001346899.1:c.2177_2179dup (EGFR) NP_001333828.1:p.Asn726_Pro727insHis
NM_001346900.1:c.2153_2155dup (EGFR) NP_001333829.1:p.Asn718_Pro719insHis
NM_001346941.1:c.1511_1513dup (EGFR) NP_001333870.1:p.Asn504_Pro505insHis
NM_005228.4:c.2312_2314dup (EGFR) NP_005219.2:p.Asn771_Pro772insHis
NM_005228.5:c.2312_2314dup (EGFR) MANE Select NP_005219.2:p.Asn771_Pro772insHis
NM_001346897.2:c.2177_2179dup (EGFR) NP_001333826.1:p.Asn726_Pro727insHis
NM_001346898.2:c.2312_2314dup (EGFR) NP_001333827.1:p.Asn771_Pro772insHis
NM_001346900.2:c.2153_2155dup (EGFR) NP_001333829.1:p.Asn718_Pro719insHis
NM_001346941.2:c.1511_1513dup (EGFR) NP_001333870.1:p.Asn504_Pro505insHis
NM_001346899.2:c.2177_2179dup (EGFR) NP_001333828.1:p.Asn726_Pro727insHis
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