Canonical Allele Identifier: CA1708918354
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174787_55174814delinsAACATCTCCGAAAGCCAACAAGGAAATC , CM000669.2:g.55174787_55174814delinsAACATCTCCGAAAGCCAACAAGGAAATC GRCh38
NC_000007.13:g.55242480_55242507delinsAACATCTCCGAAAGCCAACAAGGAAATC , CM000669.1:g.55242480_55242507delinsAACATCTCCGAAAGCCAACAAGGAAATC GRCh37
NC_000007.12:g.55209974_55210001delinsAACATCTCCGAAAGCCAACAAGGAAATC NCBI36
NG_007726.3:g.160756_160783delinsAACATCTCCGAAAGCCAACAAGGAAATC , LRG_304:g.160756_160783delinsAACATCTCCGAAAGCCAACAAGGAAATC

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2091_2118delinsAACATCTCCGAAAGCCAACAAGGAAATC ENSP00000413354.2:p.Ala697=
ENST00000700145.1:c.599_626delinsAACATCTCCGAAAGCCAACAAGGAAATC
ENST00000275493.7:c.2250_2277delinsAACATCTCCGAAAGCCAACAAGGAAATC MANE Select ENSP00000275493.2:p.Ala750=
ENST00000275493.6:c.2250_2277delinsAACATCTCCGAAAGCCAACAAGGAAATC ENSP00000275493.2:p.Ala750=
ENST00000442591.5:c.*28+1859_*28+1886delinsAACATCTCCGAAAGCCAACAAGGAAATC ENSP00000410031.1:n.*28+1859_*28+1886deli...
ENST00000454757.6:c.2115_2142delinsAACATCTCCGAAAGCCAACAAGGAAATC ENSP00000395243.3:p.Ala705=
ENST00000455089.5:c.2115_2142delinsAACATCTCCGAAAGCCAACAAGGAAATC ENSP00000415559.1:p.Ala705=
NM_005228.3:c.2250_2277delinsAACATCTCCGAAAGCCAACAAGGAAATC , LRG_304t1:c.2250_2277delinsAACATCTCCGAAAGCCAACAAGGAAATC NP_005219.2:p.Ala750=
NM_001346897.1:c.2115_2142delinsAACATCTCCGAAAGCCAACAAGGAAATC NP_001333826.1:p.Ala705=
NM_001346898.1:c.2250_2277delinsAACATCTCCGAAAGCCAACAAGGAAATC NP_001333827.1:p.Ala750=
NM_001346899.1:c.2115_2142delinsAACATCTCCGAAAGCCAACAAGGAAATC NP_001333828.1:p.Ala705=
NM_001346900.1:c.2091_2118delinsAACATCTCCGAAAGCCAACAAGGAAATC NP_001333829.1:p.Ala697=
NM_001346941.1:c.1449_1476delinsAACATCTCCGAAAGCCAACAAGGAAATC NP_001333870.1:p.Ala483=
NM_005228.4:c.2250_2277delinsAACATCTCCGAAAGCCAACAAGGAAATC NP_005219.2:p.Ala750=
NM_005228.5:c.2250_2277delinsAACATCTCCGAAAGCCAACAAGGAAATC MANE Select NP_005219.2:p.Ala750=
NM_001346897.2:c.2115_2142delinsAACATCTCCGAAAGCCAACAAGGAAATC NP_001333826.1:p.Ala705=
NM_001346898.2:c.2250_2277delinsAACATCTCCGAAAGCCAACAAGGAAATC NP_001333827.1:p.Ala750=
NM_001346900.2:c.2091_2118delinsAACATCTCCGAAAGCCAACAAGGAAATC NP_001333829.1:p.Ala697=
NM_001346941.2:c.1449_1476delinsAACATCTCCGAAAGCCAACAAGGAAATC NP_001333870.1:p.Ala483=
NM_001346899.2:c.2115_2142delinsAACATCTCCGAAAGCCAACAAGGAAATC NP_001333828.1:p.Ala705=