Canonical Allele Identifier: CA2714569377

Gene: EGFR EGFR-AS1

Linked Data

• dbSNP Id: rs1554350351

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181320_55181321insCCCCCCACGTGT , CM000669.2:g.55181320_55181321insCCCCCCACGTGT	GRCh38
NC_000007.13:g.55249013_55249014insCCCCCCACGTGT , CM000669.1:g.55249013_55249014insCCCCCCACGTGT	GRCh37
NC_000007.12:g.55216507_55216508insCCCCCCACGTGT	NCBI36
NG_007726.3:g.167289_167290insCCCCCCACGTGT , LRG_304:g.167289_167290insCCCCCCACGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2152_2153insCCCCCCACGTGT (EGFR)	ENSP00000413354.2:p.Asn718delinsThrProHisValTyr
ENST00000700145.1:c.660_661insCCCCCCACGTGT (EGFR)
ENST00000275493.7:c.2311_2312insCCCCCCACGTGT (EGFR) MANE Select	ENSP00000275493.2:p.Asn771delinsThrProHisValTyr
ENST00000275493.6:c.2311_2312insCCCCCCACGTGT (EGFR)	ENSP00000275493.2:p.Asn771delinsThrProHisValTyr
ENST00000442591.5:c.*28+8392_*28+8393insCCCCCCACGTGT (EGFR)	ENSP00000410031.1:n.*28+8392_*28+8393insCCCCCCACGTGT
ENST00000454757.6:c.2176_2177insCCCCCCACGTGT (EGFR)	ENSP00000395243.3:p.Asn726delinsThrProHisValTyr
ENST00000455089.5:c.2176_2177insCCCCCCACGTGT (EGFR)	ENSP00000415559.1:p.Asn726delinsThrProHisValTyr
NM_005228.3:c.2311_2312insCCCCCCACGTGT , LRG_304t1:c.2311_2312insCCCCCCACGTGT (EGFR)	NP_005219.2:p.Asn771delinsThrProHisValTyr
NR_047551.1:n.1250_1251insACACGTGGGGGG (EGFR-AS1)
NM_001346897.1:c.2176_2177insCCCCCCACGTGT (EGFR)	NP_001333826.1:p.Asn726delinsThrProHisValTyr
NM_001346898.1:c.2311_2312insCCCCCCACGTGT (EGFR)	NP_001333827.1:p.Asn771delinsThrProHisValTyr
NM_001346899.1:c.2176_2177insCCCCCCACGTGT (EGFR)	NP_001333828.1:p.Asn726delinsThrProHisValTyr
NM_001346900.1:c.2152_2153insCCCCCCACGTGT (EGFR)	NP_001333829.1:p.Asn718delinsThrProHisValTyr
NM_001346941.1:c.1510_1511insCCCCCCACGTGT (EGFR)	NP_001333870.1:p.Asn504delinsThrProHisValTyr
NM_005228.4:c.2311_2312insCCCCCCACGTGT (EGFR)	NP_005219.2:p.Asn771delinsThrProHisValTyr
NM_005228.5:c.2311_2312insCCCCCCACGTGT (EGFR) MANE Select	NP_005219.2:p.Asn771delinsThrProHisValTyr
NM_001346897.2:c.2176_2177insCCCCCCACGTGT (EGFR)	NP_001333826.1:p.Asn726delinsThrProHisValTyr
NM_001346898.2:c.2311_2312insCCCCCCACGTGT (EGFR)	NP_001333827.1:p.Asn771delinsThrProHisValTyr
NM_001346900.2:c.2152_2153insCCCCCCACGTGT (EGFR)	NP_001333829.1:p.Asn718delinsThrProHisValTyr
NM_001346941.2:c.1510_1511insCCCCCCACGTGT (EGFR)	NP_001333870.1:p.Asn504delinsThrProHisValTyr
NM_001346899.2:c.2176_2177insCCCCCCACGTGT (EGFR)	NP_001333828.1:p.Asn726delinsThrProHisValTyr