Canonical Allele Identifier: CA574335313

Gene: EGFR

Linked Data

• dbSNP Id: rs1318787711
• gnomAD v2: 7-55241757-C-T
• gnomAD v3: 7-55174064-C-T
• gnomAD v4: 7-55174064-C-T
• MyVariant Identifiers: chr7:g.55241757C>T (hg19) ; chr7:g.55174064C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174064C>T , CM000669.2:g.55174064C>T	GRCh38
NC_000007.13:g.55241757C>T , CM000669.1:g.55241757C>T	GRCh37
NC_000007.12:g.55209251C>T	NCBI36
NG_007726.3:g.160033C>T , LRG_304:g.160033C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2025+21C>T	ENSP00000413354.2:n.2025+21C>T
ENST00000700145.1:c.533+21C>T
ENST00000275493.7:c.2184+21C>T MANE Select	ENSP00000275493.2:n.2184+21C>T
ENST00000275493.6:c.2184+21C>T	ENSP00000275493.2:n.2184+21C>T
ENST00000442591.5:c.*28+1136C>T	ENSP00000410031.1:n.*28+1136C>T
ENST00000454757.6:c.2049+21C>T	ENSP00000395243.3:n.2049+21C>T
ENST00000455089.5:c.2049+21C>T	ENSP00000415559.1:n.2049+21C>T
NM_005228.3:c.2184+21C>T , LRG_304t1:c.2184+21C>T	NP_005219.2:n.2184+21C>T
NM_001346897.1:c.2049+21C>T	NP_001333826.1:n.2049+21C>T
NM_001346898.1:c.2184+21C>T	NP_001333827.1:n.2184+21C>T
NM_001346899.1:c.2049+21C>T	NP_001333828.1:n.2049+21C>T
NM_001346900.1:c.2025+21C>T	NP_001333829.1:n.2025+21C>T
NM_001346941.1:c.1383+21C>T	NP_001333870.1:n.1383+21C>T
NM_005228.4:c.2184+21C>T	NP_005219.2:n.2184+21C>T
NM_005228.5:c.2184+21C>T MANE Select	NP_005219.2:n.2184+21C>T
NM_001346897.2:c.2049+21C>T	NP_001333826.1:n.2049+21C>T
NM_001346898.2:c.2184+21C>T	NP_001333827.1:n.2184+21C>T
NM_001346900.2:c.2025+21C>T	NP_001333829.1:n.2025+21C>T
NM_001346941.2:c.1383+21C>T	NP_001333870.1:n.1383+21C>T
NM_001346899.2:c.2049+21C>T	NP_001333828.1:n.2049+21C>T