Canonical Allele Identifier: CA158934221

Gene: EGFR

Linked Data

• ClinVar Variation Id: 1973066
• ClinVar RCV Id: RCV002730997
• dbSNP Id: rs104886012
• gnomAD v3: 7-55191793-G-T
• gnomAD v4: 7-55191793-G-T
• MyVariant Identifiers: chr7:g.55259486G>T (hg19) ; chr7:g.55191793G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191793G>T , CM000669.2:g.55191793G>T	GRCh38
NC_000007.13:g.55259486G>T , CM000669.1:g.55259486G>T	GRCh37
NC_000007.12:g.55226980G>T	NCBI36
NG_007726.3:g.177762G>T , LRG_304:g.177762G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2385G>T	ENSP00000413354.2:p.Pro795=
ENST00000700145.1:c.893G>T
ENST00000275493.7:c.2544G>T MANE Select	ENSP00000275493.2:p.Pro848=
ENST00000275493.6:c.2544G>T	ENSP00000275493.2:p.Pro848=
ENST00000442591.5:c.*28+18865G>T	ENSP00000410031.1:n.*28+18865G>T
ENST00000454757.6:c.2409G>T	ENSP00000395243.3:p.Pro803=
ENST00000455089.5:c.2409G>T	ENSP00000415559.1:p.Pro803=
NM_005228.3:c.2544G>T , LRG_304t1:c.2544G>T	NP_005219.2:p.Pro848=
NM_001346897.1:c.2409G>T	NP_001333826.1:p.Pro803=
NM_001346898.1:c.2544G>T	NP_001333827.1:p.Pro848=
NM_001346899.1:c.2409G>T	NP_001333828.1:p.Pro803=
NM_001346900.1:c.2385G>T	NP_001333829.1:p.Pro795=
NM_001346941.1:c.1743G>T	NP_001333870.1:p.Pro581=
NM_005228.4:c.2544G>T	NP_005219.2:p.Pro848=
NM_005228.5:c.2544G>T MANE Select	NP_005219.2:p.Pro848=
NM_001346897.2:c.2409G>T	NP_001333826.1:p.Pro803=
NM_001346898.2:c.2544G>T	NP_001333827.1:p.Pro848=
NM_001346900.2:c.2385G>T	NP_001333829.1:p.Pro795=
NM_001346941.2:c.1743G>T	NP_001333870.1:p.Pro581=
NM_001346899.2:c.2409G>T	NP_001333828.1:p.Pro803=