Canonical Allele Identifier: CA367580063

Gene: EGFR

Linked Data

• dbSNP Id: rs483352808
• MyVariant Identifiers: chr7:g.55259413G>T (hg19) ; chr7:g.55191720G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191720G>T , CM000669.2:g.55191720G>T	GRCh38
NC_000007.13:g.55259413G>T , CM000669.1:g.55259413G>T	GRCh37
NC_000007.12:g.55226907G>T	NCBI36
NG_007726.3:g.177689G>T , LRG_304:g.177689G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2312G>T	ENSP00000413354.2:p.Gly771Val
ENST00000700145.1:c.820G>T
ENST00000275493.7:c.2471G>T MANE Select	ENSP00000275493.2:p.Gly824Val
ENST00000275493.6:c.2471G>T	ENSP00000275493.2:p.Gly824Val
ENST00000442591.5:c.*28+18792G>T	ENSP00000410031.1:n.*28+18792G>T
ENST00000454757.6:c.2336G>T	ENSP00000395243.3:p.Gly779Val
ENST00000455089.5:c.2336G>T	ENSP00000415559.1:p.Gly779Val
NM_005228.3:c.2471G>T , LRG_304t1:c.2471G>T	NP_005219.2:p.Gly824Val
NM_001346897.1:c.2336G>T	NP_001333826.1:p.Gly779Val
NM_001346898.1:c.2471G>T	NP_001333827.1:p.Gly824Val
NM_001346899.1:c.2336G>T	NP_001333828.1:p.Gly779Val
NM_001346900.1:c.2312G>T	NP_001333829.1:p.Gly771Val
NM_001346941.1:c.1670G>T	NP_001333870.1:p.Gly557Val
NM_005228.4:c.2471G>T	NP_005219.2:p.Gly824Val
NM_005228.5:c.2471G>T MANE Select	NP_005219.2:p.Gly824Val
NM_001346897.2:c.2336G>T	NP_001333826.1:p.Gly779Val
NM_001346898.2:c.2471G>T	NP_001333827.1:p.Gly824Val
NM_001346900.2:c.2312G>T	NP_001333829.1:p.Gly771Val
NM_001346941.2:c.1670G>T	NP_001333870.1:p.Gly557Val
NM_001346899.2:c.2336G>T	NP_001333828.1:p.Gly779Val