Canonical Allele Identifier: CA367582582

Gene: EGFR

Linked Data

• MyVariant Identifiers: chr7:g.55268993A>C (hg19) ; chr7:g.55201300A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55201300A>C , CM000669.2:g.55201300A>C	GRCh38
NC_000007.13:g.55268993A>C , CM000669.1:g.55268993A>C	GRCh37
NC_000007.12:g.55236487A>C	NCBI36
NG_007726.3:g.187269A>C , LRG_304:g.187269A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2900A>C	ENSP00000413354.2:p.Gln967Pro
ENST00000700145.1:c.900-4047A>C
ENST00000700146.1:n.803A>C
ENST00000700147.1:n.728A>C
ENST00000275493.7:c.3059A>C MANE Select	ENSP00000275493.2:p.Gln1020Pro
ENST00000275493.6:c.3059A>C	ENSP00000275493.2:p.Gln1020Pro
ENST00000442591.5:c.*28+28372A>C	ENSP00000410031.1:n.*28+28372A>C
ENST00000454757.6:c.2924A>C	ENSP00000395243.3:p.Gln975Pro
ENST00000455089.5:c.2924A>C	ENSP00000415559.1:p.Gln975Pro
NM_005228.3:c.3059A>C , LRG_304t1:c.3059A>C	NP_005219.2:p.Gln1020Pro
NM_001346897.1:c.2924A>C	NP_001333826.1:p.Gln975Pro
NM_001346898.1:c.3059A>C	NP_001333827.1:p.Gln1020Pro
NM_001346899.1:c.2924A>C	NP_001333828.1:p.Gln975Pro
NM_001346900.1:c.2900A>C	NP_001333829.1:p.Gln967Pro
NM_001346941.1:c.2258A>C	NP_001333870.1:p.Gln753Pro
NM_005228.4:c.3059A>C	NP_005219.2:p.Gln1020Pro
NM_005228.5:c.3059A>C MANE Select	NP_005219.2:p.Gln1020Pro
NM_001346897.2:c.2924A>C	NP_001333826.1:p.Gln975Pro
NM_001346898.2:c.3059A>C	NP_001333827.1:p.Gln1020Pro
NM_001346900.2:c.2900A>C	NP_001333829.1:p.Gln967Pro
NM_001346941.2:c.2258A>C	NP_001333870.1:p.Gln753Pro
NM_001346899.2:c.2924A>C	NP_001333828.1:p.Gln975Pro