Canonical Allele Identifier: CA454965594

Gene: EGFR

Linked Data

• dbSNP Id: rs2128964435
• MyVariant Identifiers: chr7:g.55259444G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191751G>A , CM000669.2:g.55191751G>A	GRCh38
NC_000007.13:g.55259444G>A , CM000669.1:g.55259444G>A	GRCh37
NC_000007.12:g.55226938G>A	NCBI36
NG_007726.3:g.177720G>A , LRG_304:g.177720G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2343G>A	ENSP00000413354.2:p.Val781=
ENST00000700145.1:c.851G>A
ENST00000275493.7:c.2502G>A MANE Select	ENSP00000275493.2:p.Val834=
ENST00000275493.6:c.2502G>A	ENSP00000275493.2:p.Val834=
ENST00000442591.5:c.*28+18823G>A	ENSP00000410031.1:n.*28+18823G>A
ENST00000454757.6:c.2367G>A	ENSP00000395243.3:p.Val789=
ENST00000455089.5:c.2367G>A	ENSP00000415559.1:p.Val789=
NM_005228.3:c.2502G>A , LRG_304t1:c.2502G>A	NP_005219.2:p.Val834=
NM_001346897.1:c.2367G>A	NP_001333826.1:p.Val789=
NM_001346898.1:c.2502G>A	NP_001333827.1:p.Val834=
NM_001346899.1:c.2367G>A	NP_001333828.1:p.Val789=
NM_001346900.1:c.2343G>A	NP_001333829.1:p.Val781=
NM_001346941.1:c.1701G>A	NP_001333870.1:p.Val567=
NM_005228.4:c.2502G>A	NP_005219.2:p.Val834=
NM_005228.5:c.2502G>A MANE Select	NP_005219.2:p.Val834=
NM_001346897.2:c.2367G>A	NP_001333826.1:p.Val789=
NM_001346898.2:c.2502G>A	NP_001333827.1:p.Val834=
NM_001346900.2:c.2343G>A	NP_001333829.1:p.Val781=
NM_001346941.2:c.1701G>A	NP_001333870.1:p.Val567=
NM_001346899.2:c.2367G>A	NP_001333828.1:p.Val789=