Canonical Allele Identifier: CA1708905076

Gene: EGFR EGFR-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181312_55181313delinsGC , CM000669.2:g.55181312_55181313delinsGC	GRCh38
NC_000007.13:g.55249005_55249006delinsGC , CM000669.1:g.55249005_55249006delinsGC	GRCh37
NC_000007.12:g.55216499_55216500delinsGC	NCBI36
NG_007726.3:g.167281_167282delinsGC , LRG_304:g.167281_167282delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2144_2145delinsGC (EGFR)	ENSP00000413354.2:p.Ser715=
ENST00000700145.1:c.652_653delinsGC (EGFR)
ENST00000275493.7:c.2303_2304delinsGC (EGFR) MANE Select	ENSP00000275493.2:p.Ser768=
ENST00000275493.6:c.2303_2304delinsGC (EGFR)	ENSP00000275493.2:p.Ser768=
ENST00000442591.5:c.*28+8384_*28+8385delinsGC (EGFR)	ENSP00000410031.1:n.*28+8384_*28+8385deli...
ENST00000454757.6:c.2168_2169delinsGC (EGFR)	ENSP00000395243.3:p.Ser723=
ENST00000455089.5:c.2168_2169delinsGC (EGFR)	ENSP00000415559.1:p.Ser723=
NM_005228.3:c.2303_2304delinsGC , LRG_304t1:c.2303_2304delinsGC (EGFR)	NP_005219.2:p.Ser768=
NR_047551.1:n.1258_1259delinsGC (EGFR-AS1)
NM_001346897.1:c.2168_2169delinsGC (EGFR)	NP_001333826.1:p.Ser723=
NM_001346898.1:c.2303_2304delinsGC (EGFR)	NP_001333827.1:p.Ser768=
NM_001346899.1:c.2168_2169delinsGC (EGFR)	NP_001333828.1:p.Ser723=
NM_001346900.1:c.2144_2145delinsGC (EGFR)	NP_001333829.1:p.Ser715=
NM_001346941.1:c.1502_1503delinsGC (EGFR)	NP_001333870.1:p.Ser501=
NM_005228.4:c.2303_2304delinsGC (EGFR)	NP_005219.2:p.Ser768=
NM_005228.5:c.2303_2304delinsGC (EGFR) MANE Select	NP_005219.2:p.Ser768=
NM_001346897.2:c.2168_2169delinsGC (EGFR)	NP_001333826.1:p.Ser723=
NM_001346898.2:c.2303_2304delinsGC (EGFR)	NP_001333827.1:p.Ser768=
NM_001346900.2:c.2144_2145delinsGC (EGFR)	NP_001333829.1:p.Ser715=
NM_001346941.2:c.1502_1503delinsGC (EGFR)	NP_001333870.1:p.Ser501=
NM_001346899.2:c.2168_2169delinsGC (EGFR)	NP_001333828.1:p.Ser723=