Canonical Allele Identifier: CA367582421

Gene: EGFR

Linked Data

• dbSNP Id: rs771085105
• MyVariant Identifiers: chr7:g.55268922C>G (hg19) ; chr7:g.55201229C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55201229C>G , CM000669.2:g.55201229C>G	GRCh38
NC_000007.13:g.55268922C>G , CM000669.1:g.55268922C>G	GRCh37
NC_000007.12:g.55236416C>G	NCBI36
NG_007726.3:g.187198C>G , LRG_304:g.187198C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2829C>G	ENSP00000413354.2:p.Asn943Lys
ENST00000700145.1:c.900-4118C>G
ENST00000700146.1:n.732C>G
ENST00000700147.1:n.657C>G
ENST00000275493.7:c.2988C>G MANE Select	ENSP00000275493.2:p.Asn996Lys
ENST00000275493.6:c.2988C>G	ENSP00000275493.2:p.Asn996Lys
ENST00000442591.5:c.*28+28301C>G	ENSP00000410031.1:n.*28+28301C>G
ENST00000454757.6:c.2853C>G	ENSP00000395243.3:p.Asn951Lys
ENST00000455089.5:c.2853C>G	ENSP00000415559.1:p.Asn951Lys
NM_005228.3:c.2988C>G , LRG_304t1:c.2988C>G	NP_005219.2:p.Asn996Lys
NM_001346897.1:c.2853C>G	NP_001333826.1:p.Asn951Lys
NM_001346898.1:c.2988C>G	NP_001333827.1:p.Asn996Lys
NM_001346899.1:c.2853C>G	NP_001333828.1:p.Asn951Lys
NM_001346900.1:c.2829C>G	NP_001333829.1:p.Asn943Lys
NM_001346941.1:c.2187C>G	NP_001333870.1:p.Asn729Lys
NM_005228.4:c.2988C>G	NP_005219.2:p.Asn996Lys
NM_005228.5:c.2988C>G MANE Select	NP_005219.2:p.Asn996Lys
NM_001346897.2:c.2853C>G	NP_001333826.1:p.Asn951Lys
NM_001346898.2:c.2988C>G	NP_001333827.1:p.Asn996Lys
NM_001346900.2:c.2829C>G	NP_001333829.1:p.Asn943Lys
NM_001346941.2:c.2187C>G	NP_001333870.1:p.Asn729Lys
NM_001346899.2:c.2853C>G	NP_001333828.1:p.Asn951Lys