Canonical Allele Identifier: CA2838010099
Gene: EGFR HGNC NCBI
EGFR-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55181311_55181338del , CM000669.2:g.55181311_55181338del GRCh38
NC_000007.13:g.55249004_55249031del , CM000669.1:g.55249004_55249031del GRCh37
NC_000007.12:g.55216498_55216525del NCBI36
NG_007726.3:g.167280_167307del , LRG_304:g.167280_167307del

Transcript Alleles

HGVS Amino-acid Change
ENST00000450046.2:c.2143_2170del (EGFR) ENSP00000413354.2:p.Ser715CysfsTer?
ENST00000700145.1:c.651_678del (EGFR)
ENST00000275493.7:c.2302_2329del (EGFR) MANE Select ENSP00000275493.2:p.Ser768CysfsTer?
ENST00000275493.6:c.2302_2329del (EGFR) ENSP00000275493.2:p.Ser768CysfsTer?
ENST00000442591.5:c.*28+8383_*28+8410del (EGFR) ENSP00000410031.1:n.*28+8383_*28+8410del
ENST00000454757.6:c.2167_2194del (EGFR) ENSP00000395243.3:p.Ser723CysfsTer?
ENST00000455089.5:c.2167_2194del (EGFR) ENSP00000415559.1:p.Ser723CysfsTer?
NM_005228.3:c.2302_2329del , LRG_304t1:c.2302_2329del (EGFR) NP_005219.2:p.Ser768CysfsTer?
NR_047551.1:n.1236_1263del (EGFR-AS1)
NM_001346897.1:c.2167_2194del (EGFR) NP_001333826.1:p.Ser723CysfsTer?
NM_001346898.1:c.2302_2329del (EGFR) NP_001333827.1:p.Ser768CysfsTer?
NM_001346899.1:c.2167_2194del (EGFR) NP_001333828.1:p.Ser723CysfsTer?
NM_001346900.1:c.2143_2170del (EGFR) NP_001333829.1:p.Ser715CysfsTer?
NM_001346941.1:c.1501_1528del (EGFR) NP_001333870.1:p.Ser501CysfsTer?
NM_005228.4:c.2302_2329del (EGFR) NP_005219.2:p.Ser768CysfsTer?
NM_005228.5:c.2302_2329del (EGFR) MANE Select NP_005219.2:p.Ser768CysfsTer?
NM_001346897.2:c.2167_2194del (EGFR) NP_001333826.1:p.Ser723CysfsTer?
NM_001346898.2:c.2302_2329del (EGFR) NP_001333827.1:p.Ser768CysfsTer?
NM_001346900.2:c.2143_2170del (EGFR) NP_001333829.1:p.Ser715CysfsTer?
NM_001346941.2:c.1501_1528del (EGFR) NP_001333870.1:p.Ser501CysfsTer?
NM_001346899.2:c.2167_2194del (EGFR) NP_001333828.1:p.Ser723CysfsTer?