Canonical Allele Identifier: CA158928400

Gene: EGFR EGFR-AS1

Linked Data

• dbSNP Id: rs761020556
• MyVariant Identifiers: chr7:g.55249018C>G (hg19) ; chr7:g.55181325C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181325C>G , CM000669.2:g.55181325C>G	GRCh38
NC_000007.13:g.55249018C>G , CM000669.1:g.55249018C>G	GRCh37
NC_000007.12:g.55216512C>G	NCBI36
NG_007726.3:g.167294C>G , LRG_304:g.167294C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2157C>G (EGFR)	ENSP00000413354.2:p.Pro719=
ENST00000700145.1:c.665C>G (EGFR)
ENST00000275493.7:c.2316C>G (EGFR) MANE Select	ENSP00000275493.2:p.Pro772=
ENST00000275493.6:c.2316C>G (EGFR)	ENSP00000275493.2:p.Pro772=
ENST00000442591.5:c.*28+8397C>G (EGFR)	ENSP00000410031.1:n.*28+8397C>G
ENST00000454757.6:c.2181C>G (EGFR)	ENSP00000395243.3:p.Pro727=
ENST00000455089.5:c.2181C>G (EGFR)	ENSP00000415559.1:p.Pro727=
NM_005228.3:c.2316C>G , LRG_304t1:c.2316C>G (EGFR)	NP_005219.2:p.Pro772=
NR_047551.1:n.1246G>C (EGFR-AS1)
NM_001346897.1:c.2181C>G (EGFR)	NP_001333826.1:p.Pro727=
NM_001346898.1:c.2316C>G (EGFR)	NP_001333827.1:p.Pro772=
NM_001346899.1:c.2181C>G (EGFR)	NP_001333828.1:p.Pro727=
NM_001346900.1:c.2157C>G (EGFR)	NP_001333829.1:p.Pro719=
NM_001346941.1:c.1515C>G (EGFR)	NP_001333870.1:p.Pro505=
NM_005228.4:c.2316C>G (EGFR)	NP_005219.2:p.Pro772=
NM_005228.5:c.2316C>G (EGFR) MANE Select	NP_005219.2:p.Pro772=
NM_001346897.2:c.2181C>G (EGFR)	NP_001333826.1:p.Pro727=
NM_001346898.2:c.2316C>G (EGFR)	NP_001333827.1:p.Pro772=
NM_001346900.2:c.2157C>G (EGFR)	NP_001333829.1:p.Pro719=
NM_001346941.2:c.1515C>G (EGFR)	NP_001333870.1:p.Pro505=
NM_001346899.2:c.2181C>G (EGFR)	NP_001333828.1:p.Pro727=