Canonical Allele Identifier: CA4265363

Gene: EGFR

Linked Data

• ClinVar Variation Id: 1102720
• ClinVar RCV Id: RCV002258249
• dbSNP Id: rs751873368
• ExAC: 7:55221733 G / A
• gnomAD v2: 7-55221733-G-A
• gnomAD v3: 7-55154040-G-A
• gnomAD v4: 7-55154040-G-A
• COSMIC: COSM3266553 ; COSM3266554
• MyVariant Identifiers: chr7:g.55221733G>A (hg19) ; chr7:g.55154040G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55154040G>A , CM000669.2:g.55154040G>A	GRCh38
NC_000007.13:g.55221733G>A , CM000669.1:g.55221733G>A	GRCh37
NC_000007.12:g.55189227G>A	NCBI36
NG_007726.3:g.140009G>A , LRG_304:g.140009G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.618G>A	ENSP00000413354.2:p.Thr206=
ENST00000700144.1:n.967G>A
ENST00000344576.7:c.777G>A	ENSP00000345973.2:p.Thr259=
ENST00000275493.7:c.777G>A MANE Select	ENSP00000275493.2:p.Thr259=
ENST00000275493.6:c.777G>A	ENSP00000275493.2:p.Thr259=
ENST00000342916.7:c.777G>A	ENSP00000342376.3:p.Thr259=
ENST00000344576.6:c.777G>A	ENSP00000345973.2:p.Thr259=
ENST00000420316.6:c.777G>A	ENSP00000413843.2:p.Thr259=
ENST00000442591.5:c.777G>A	ENSP00000410031.1:p.Thr259=
ENST00000454757.6:c.642G>A	ENSP00000395243.3:p.Thr214=
ENST00000455089.5:c.642G>A	ENSP00000415559.1:p.Thr214=
NM_005228.3:c.777G>A , LRG_304t1:c.777G>A	NP_005219.2:p.Thr259=
NM_201282.1:c.777G>A	NP_958439.1:p.Thr259=
NM_201283.1:c.777G>A	NP_958440.1:p.Thr259=
NM_201284.1:c.777G>A	NP_958441.1:p.Thr259=
NM_001346897.1:c.642G>A	NP_001333826.1:p.Thr214=
NM_001346898.1:c.777G>A	NP_001333827.1:p.Thr259=
NM_001346899.1:c.642G>A	NP_001333828.1:p.Thr214=
NM_001346900.1:c.618G>A	NP_001333829.1:p.Thr206=
NM_001346941.1:c.89-1790G>A	NP_001333870.1:n.89-1790G>A
NM_005228.4:c.777G>A	NP_005219.2:p.Thr259=
NM_005228.5:c.777G>A MANE Select	NP_005219.2:p.Thr259=
NM_001346897.2:c.642G>A	NP_001333826.1:p.Thr214=
NM_001346898.2:c.777G>A	NP_001333827.1:p.Thr259=
NM_001346900.2:c.618G>A	NP_001333829.1:p.Thr206=
NM_001346941.2:c.89-1790G>A	NP_001333870.1:n.89-1790G>A
NM_201282.2:c.777G>A	NP_958439.1:p.Thr259=
NM_201284.2:c.777G>A	NP_958441.1:p.Thr259=
NM_001346899.2:c.642G>A	NP_001333828.1:p.Thr214=
NM_201283.2:c.777G>A	NP_958440.1:p.Thr259=