Canonical Allele Identifier: CA135884

Gene: EGFR EGFR-AS1

Linked Data

• ClinVar Variation Id: 45267
• ClinVar RCV Id: RCV000038423
• dbSNP Id: rs397517120
• MyVariant Identifiers: chr7:g.55249038G>T (hg19) ; chr7:g.55181345G>T (hg38)
• PubMed: PMID:15788655 ; PMID:16467085

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181345G>T , CM000669.2:g.55181345G>T	GRCh38
NC_000007.13:g.55249038G>T , CM000669.1:g.55249038G>T	GRCh37
NC_000007.12:g.55216532G>T	NCBI36
NG_007726.3:g.167314G>T , LRG_304:g.167314G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2177G>T (EGFR)	ENSP00000413354.2:p.Gly726Val
ENST00000700145.1:c.685G>T (EGFR)
ENST00000275493.7:c.2336G>T (EGFR) MANE Select	ENSP00000275493.2:p.Gly779Val
ENST00000275493.6:c.2336G>T (EGFR)	ENSP00000275493.2:p.Gly779Val
ENST00000442591.5:c.*28+8417G>T (EGFR)	ENSP00000410031.1:n.*28+8417G>T
ENST00000454757.6:c.2201G>T (EGFR)	ENSP00000395243.3:p.Gly734Val
ENST00000455089.5:c.2201G>T (EGFR)	ENSP00000415559.1:p.Gly734Val
NM_005228.3:c.2336G>T , LRG_304t1:c.2336G>T (EGFR)	NP_005219.2:p.Gly779Val
NR_047551.1:n.1226C>A (EGFR-AS1)
NM_001346897.1:c.2201G>T (EGFR)	NP_001333826.1:p.Gly734Val
NM_001346898.1:c.2336G>T (EGFR)	NP_001333827.1:p.Gly779Val
NM_001346899.1:c.2201G>T (EGFR)	NP_001333828.1:p.Gly734Val
NM_001346900.1:c.2177G>T (EGFR)	NP_001333829.1:p.Gly726Val
NM_001346941.1:c.1535G>T (EGFR)	NP_001333870.1:p.Gly512Val
NM_005228.4:c.2336G>T (EGFR)	NP_005219.2:p.Gly779Val
NM_005228.5:c.2336G>T (EGFR) MANE Select	NP_005219.2:p.Gly779Val
NM_001346897.2:c.2201G>T (EGFR)	NP_001333826.1:p.Gly734Val
NM_001346898.2:c.2336G>T (EGFR)	NP_001333827.1:p.Gly779Val
NM_001346900.2:c.2177G>T (EGFR)	NP_001333829.1:p.Gly726Val
NM_001346941.2:c.1535G>T (EGFR)	NP_001333870.1:p.Gly512Val
NM_001346899.2:c.2201G>T (EGFR)	NP_001333828.1:p.Gly734Val