Canonical Allele Identifier: CA1708909790
Gene: EGFR HGNC NCBI
EGFR-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55183709_55183712delinsTTTC , CM000669.2:g.55183709_55183712delinsTTTC GRCh38
NC_000007.13:g.55251402_55251405delinsTTTC , CM000669.1:g.55251402_55251405delinsTTTC GRCh37
NC_000007.12:g.55218896_55218899delinsTTTC NCBI36
NG_007726.3:g.169678_169681delinsTTTC , LRG_304:g.169678_169681delinsTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000450046.2:c.2310+2231_2310+2234delinsTTTC (EGFR) ENSP00000413354.2:n.2310+2231_2310+2234delinsTTTC
ENST00000700145.1:c.818+2231_818+2234delinsTTTC (EGFR)
ENST00000275493.7:c.2469+2231_2469+2234delinsTTTC (EGFR) MANE Select ENSP00000275493.2:n.2469+2231_2469+2234delinsTTTC
ENST00000275493.6:c.2469+2231_2469+2234delinsTTTC (EGFR) ENSP00000275493.2:n.2469+2231_2469+2234delinsTTTC
ENST00000442591.5:c.*28+10781_*28+10784delinsTTTC (EGFR) ENSP00000410031.1:n.*28+10781_*28+10784delinsTTTC
ENST00000454757.6:c.2334+2231_2334+2234delinsTTTC (EGFR) ENSP00000395243.3:n.2334+2231_2334+2234delinsTTTC
ENST00000455089.5:c.2334+2231_2334+2234delinsTTTC (EGFR) ENSP00000415559.1:n.2334+2231_2334+2234delinsTTTC
NM_005228.3:c.2469+2231_2469+2234delinsTTTC , LRG_304t1:c.2469+2231_2469+2234delinsTTTC (EGFR) NP_005219.2:n.2469+2231_2469+2234delinsTTTC
NR_047551.1:n.94-1235_94-1232delinsGAAA (EGFR-AS1)
NM_001346897.1:c.2334+2231_2334+2234delinsTTTC (EGFR) NP_001333826.1:n.2334+2231_2334+2234delinsTTTC
NM_001346898.1:c.2469+2231_2469+2234delinsTTTC (EGFR) NP_001333827.1:n.2469+2231_2469+2234delinsTTTC
NM_001346899.1:c.2334+2231_2334+2234delinsTTTC (EGFR) NP_001333828.1:n.2334+2231_2334+2234delinsTTTC
NM_001346900.1:c.2310+2231_2310+2234delinsTTTC (EGFR) NP_001333829.1:n.2310+2231_2310+2234delinsTTTC
NM_001346941.1:c.1668+2231_1668+2234delinsTTTC (EGFR) NP_001333870.1:n.1668+2231_1668+2234delinsTTTC
NM_005228.4:c.2469+2231_2469+2234delinsTTTC (EGFR) NP_005219.2:n.2469+2231_2469+2234delinsTTTC
NM_005228.5:c.2469+2231_2469+2234delinsTTTC (EGFR) MANE Select NP_005219.2:n.2469+2231_2469+2234delinsTTTC
NM_001346897.2:c.2334+2231_2334+2234delinsTTTC (EGFR) NP_001333826.1:n.2334+2231_2334+2234delinsTTTC
NM_001346898.2:c.2469+2231_2469+2234delinsTTTC (EGFR) NP_001333827.1:n.2469+2231_2469+2234delinsTTTC
NM_001346900.2:c.2310+2231_2310+2234delinsTTTC (EGFR) NP_001333829.1:n.2310+2231_2310+2234delinsTTTC
NM_001346941.2:c.1668+2231_1668+2234delinsTTTC (EGFR) NP_001333870.1:n.1668+2231_1668+2234delinsTTTC
NM_001346899.2:c.2334+2231_2334+2234delinsTTTC (EGFR) NP_001333828.1:n.2334+2231_2334+2234delinsTTTC