Canonical Allele Identifier: CA2573142228

Gene: EGFR

Linked Data

• ClinVar Variation Id: 1571935
• ClinVar RCV Id: RCV002219393
• dbSNP Id: rs2128964324

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191708C>T , CM000669.2:g.55191708C>T	GRCh38
NC_000007.13:g.55259401C>T , CM000669.1:g.55259401C>T	GRCh37
NC_000007.12:g.55226895C>T	NCBI36
NG_007726.3:g.177677C>T , LRG_304:g.177677C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2311-11C>T	ENSP00000413354.2:n.2311-11C>T
ENST00000700145.1:c.819-11C>T
ENST00000275493.7:c.2470-11C>T MANE Select	ENSP00000275493.2:n.2470-11C>T
ENST00000275493.6:c.2470-11C>T	ENSP00000275493.2:n.2470-11C>T
ENST00000442591.5:c.*28+18780C>T	ENSP00000410031.1:n.*28+18780C>T
ENST00000454757.6:c.2335-11C>T	ENSP00000395243.3:n.2335-11C>T
ENST00000455089.5:c.2335-11C>T	ENSP00000415559.1:n.2335-11C>T
NM_005228.3:c.2470-11C>T , LRG_304t1:c.2470-11C>T	NP_005219.2:n.2470-11C>T
NM_001346897.1:c.2335-11C>T	NP_001333826.1:n.2335-11C>T
NM_001346898.1:c.2470-11C>T	NP_001333827.1:n.2470-11C>T
NM_001346899.1:c.2335-11C>T	NP_001333828.1:n.2335-11C>T
NM_001346900.1:c.2311-11C>T	NP_001333829.1:n.2311-11C>T
NM_001346941.1:c.1669-11C>T	NP_001333870.1:n.1669-11C>T
NM_005228.4:c.2470-11C>T	NP_005219.2:n.2470-11C>T
NM_005228.5:c.2470-11C>T MANE Select	NP_005219.2:n.2470-11C>T
NM_001346897.2:c.2335-11C>T	NP_001333826.1:n.2335-11C>T
NM_001346898.2:c.2470-11C>T	NP_001333827.1:n.2470-11C>T
NM_001346900.2:c.2311-11C>T	NP_001333829.1:n.2311-11C>T
NM_001346941.2:c.1669-11C>T	NP_001333870.1:n.1669-11C>T
NM_001346899.2:c.2335-11C>T	NP_001333828.1:n.2335-11C>T