Canonical Allele Identifier: CA367579029

Gene: EGFR EGFR-AS1

Linked Data

• MyVariant Identifiers: chr7:g.55249151T>C (hg19) ; chr7:g.55181458T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181458T>C , CM000669.2:g.55181458T>C	GRCh38
NC_000007.13:g.55249151T>C , CM000669.1:g.55249151T>C	GRCh37
NC_000007.12:g.55216645T>C	NCBI36
NG_007726.3:g.167427T>C , LRG_304:g.167427T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2290T>C (EGFR)	ENSP00000413354.2:p.Trp764Arg
ENST00000700145.1:c.798T>C (EGFR)
ENST00000275493.7:c.2449T>C (EGFR) MANE Select	ENSP00000275493.2:p.Trp817Arg
ENST00000275493.6:c.2449T>C (EGFR)	ENSP00000275493.2:p.Trp817Arg
ENST00000442591.5:c.*28+8530T>C (EGFR)	ENSP00000410031.1:n.*28+8530T>C
ENST00000454757.6:c.2314T>C (EGFR)	ENSP00000395243.3:p.Trp772Arg
ENST00000455089.5:c.2314T>C (EGFR)	ENSP00000415559.1:p.Trp772Arg
NM_005228.3:c.2449T>C , LRG_304t1:c.2449T>C (EGFR)	NP_005219.2:p.Trp817Arg
NR_047551.1:n.1113A>G (EGFR-AS1)
NM_001346897.1:c.2314T>C (EGFR)	NP_001333826.1:p.Trp772Arg
NM_001346898.1:c.2449T>C (EGFR)	NP_001333827.1:p.Trp817Arg
NM_001346899.1:c.2314T>C (EGFR)	NP_001333828.1:p.Trp772Arg
NM_001346900.1:c.2290T>C (EGFR)	NP_001333829.1:p.Trp764Arg
NM_001346941.1:c.1648T>C (EGFR)	NP_001333870.1:p.Trp550Arg
NM_005228.4:c.2449T>C (EGFR)	NP_005219.2:p.Trp817Arg
NM_005228.5:c.2449T>C (EGFR) MANE Select	NP_005219.2:p.Trp817Arg
NM_001346897.2:c.2314T>C (EGFR)	NP_001333826.1:p.Trp772Arg
NM_001346898.2:c.2449T>C (EGFR)	NP_001333827.1:p.Trp817Arg
NM_001346900.2:c.2290T>C (EGFR)	NP_001333829.1:p.Trp764Arg
NM_001346941.2:c.1648T>C (EGFR)	NP_001333870.1:p.Trp550Arg
NM_001346899.2:c.2314T>C (EGFR)	NP_001333828.1:p.Trp772Arg