Canonical Allele Identifier: CA367576828

Gene: EGFR

Linked Data

• MyVariant Identifiers: chr7:g.55219007T>C (hg19) ; chr7:g.55151314T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55151314T>C , CM000669.2:g.55151314T>C	GRCh38
NC_000007.13:g.55219007T>C , CM000669.1:g.55219007T>C	GRCh37
NC_000007.12:g.55186501T>C	NCBI36
NG_007726.3:g.137283T>C , LRG_304:g.137283T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.421T>C	ENSP00000413354.2:p.Cys141Arg
ENST00000700144.1:n.770T>C
ENST00000344576.7:c.580T>C	ENSP00000345973.2:p.Cys194Arg
ENST00000275493.7:c.580T>C MANE Select	ENSP00000275493.2:p.Cys194Arg
ENST00000275493.6:c.580T>C	ENSP00000275493.2:p.Cys194Arg
ENST00000342916.7:c.580T>C	ENSP00000342376.3:p.Cys194Arg
ENST00000344576.6:c.580T>C	ENSP00000345973.2:p.Cys194Arg
ENST00000420316.6:c.580T>C	ENSP00000413843.2:p.Cys194Arg
ENST00000442591.5:c.580T>C	ENSP00000410031.1:p.Cys194Arg
ENST00000454757.6:c.445T>C	ENSP00000395243.3:p.Cys149Arg
ENST00000455089.5:c.445T>C	ENSP00000415559.1:p.Cys149Arg
NM_005228.3:c.580T>C , LRG_304t1:c.580T>C	NP_005219.2:p.Cys194Arg
NM_201282.1:c.580T>C	NP_958439.1:p.Cys194Arg
NM_201283.1:c.580T>C	NP_958440.1:p.Cys194Arg
NM_201284.1:c.580T>C	NP_958441.1:p.Cys194Arg
NM_001346897.1:c.445T>C	NP_001333826.1:p.Cys149Arg
NM_001346898.1:c.580T>C	NP_001333827.1:p.Cys194Arg
NM_001346899.1:c.445T>C	NP_001333828.1:p.Cys149Arg
NM_001346900.1:c.421T>C	NP_001333829.1:p.Cys141Arg
NM_001346941.1:c.89-4516T>C	NP_001333870.1:n.89-4516T>C
NM_005228.4:c.580T>C	NP_005219.2:p.Cys194Arg
NM_005228.5:c.580T>C MANE Select	NP_005219.2:p.Cys194Arg
NM_001346897.2:c.445T>C	NP_001333826.1:p.Cys149Arg
NM_001346898.2:c.580T>C	NP_001333827.1:p.Cys194Arg
NM_001346900.2:c.421T>C	NP_001333829.1:p.Cys141Arg
NM_001346941.2:c.89-4516T>C	NP_001333870.1:n.89-4516T>C
NM_201282.2:c.580T>C	NP_958439.1:p.Cys194Arg
NM_201284.2:c.580T>C	NP_958441.1:p.Cys194Arg
NM_001346899.2:c.445T>C	NP_001333828.1:p.Cys149Arg
NM_201283.2:c.580T>C	NP_958440.1:p.Cys194Arg