Canonical Allele Identifier: CA367584071

Gene: EGFR

Linked Data

• dbSNP Id: rs2128954638
• MyVariant Identifiers: chr7:g.55242446A>G (hg19) ; chr7:g.55174753A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174753A>G , CM000669.2:g.55174753A>G	GRCh38
NC_000007.13:g.55242446A>G , CM000669.1:g.55242446A>G	GRCh37
NC_000007.12:g.55209940A>G	NCBI36
NG_007726.3:g.160722A>G , LRG_304:g.160722A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2057A>G	ENSP00000413354.2:p.Lys686Arg
ENST00000700145.1:c.565A>G
ENST00000275493.7:c.2216A>G MANE Select	ENSP00000275493.2:p.Lys739Arg
ENST00000275493.6:c.2216A>G	ENSP00000275493.2:p.Lys739Arg
ENST00000442591.5:c.*28+1825A>G	ENSP00000410031.1:n.*28+1825A>G
ENST00000454757.6:c.2081A>G	ENSP00000395243.3:p.Lys694Arg
ENST00000455089.5:c.2081A>G	ENSP00000415559.1:p.Lys694Arg
NM_005228.3:c.2216A>G , LRG_304t1:c.2216A>G	NP_005219.2:p.Lys739Arg
NM_001346897.1:c.2081A>G	NP_001333826.1:p.Lys694Arg
NM_001346898.1:c.2216A>G	NP_001333827.1:p.Lys739Arg
NM_001346899.1:c.2081A>G	NP_001333828.1:p.Lys694Arg
NM_001346900.1:c.2057A>G	NP_001333829.1:p.Lys686Arg
NM_001346941.1:c.1415A>G	NP_001333870.1:p.Lys472Arg
NM_005228.4:c.2216A>G	NP_005219.2:p.Lys739Arg
NM_005228.5:c.2216A>G MANE Select	NP_005219.2:p.Lys739Arg
NM_001346897.2:c.2081A>G	NP_001333826.1:p.Lys694Arg
NM_001346898.2:c.2216A>G	NP_001333827.1:p.Lys739Arg
NM_001346900.2:c.2057A>G	NP_001333829.1:p.Lys686Arg
NM_001346941.2:c.1415A>G	NP_001333870.1:p.Lys472Arg
NM_001346899.2:c.2081A>G	NP_001333828.1:p.Lys694Arg