Canonical Allele Identifier: CA4266058

Gene: EGFR EGFR-AS1

Linked Data

• ClinVar Variation Id: 935267
• ClinVar RCV Id: RCV001203822
• dbSNP Id: rs762672864
• ExAC: 7:55249058 G / A
• gnomAD v2: 7-55249058-G-A
• gnomAD v3: 7-55181365-G-A
• gnomAD v4: 7-55181365-G-A
• COSMIC: COSM27110
• MyVariant Identifiers: chr7:g.55249058G>A (hg19) ; chr7:g.55181365G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181365G>A , CM000669.2:g.55181365G>A	GRCh38
NC_000007.13:g.55249058G>A , CM000669.1:g.55249058G>A	GRCh37
NC_000007.12:g.55216552G>A	NCBI36
NG_007726.3:g.167334G>A , LRG_304:g.167334G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2197G>A (EGFR)	ENSP00000413354.2:p.Val733Met
ENST00000700145.1:c.705G>A (EGFR)
ENST00000275493.7:c.2356G>A (EGFR) MANE Select	ENSP00000275493.2:p.Val786Met
ENST00000275493.6:c.2356G>A (EGFR)	ENSP00000275493.2:p.Val786Met
ENST00000442591.5:c.*28+8437G>A (EGFR)	ENSP00000410031.1:n.*28+8437G>A
ENST00000454757.6:c.2221G>A (EGFR)	ENSP00000395243.3:p.Val741Met
ENST00000455089.5:c.2221G>A (EGFR)	ENSP00000415559.1:p.Val741Met
NM_005228.3:c.2356G>A , LRG_304t1:c.2356G>A (EGFR)	NP_005219.2:p.Val786Met
NR_047551.1:n.1206C>T (EGFR-AS1)
NM_001346897.1:c.2221G>A (EGFR)	NP_001333826.1:p.Val741Met
NM_001346898.1:c.2356G>A (EGFR)	NP_001333827.1:p.Val786Met
NM_001346899.1:c.2221G>A (EGFR)	NP_001333828.1:p.Val741Met
NM_001346900.1:c.2197G>A (EGFR)	NP_001333829.1:p.Val733Met
NM_001346941.1:c.1555G>A (EGFR)	NP_001333870.1:p.Val519Met
NM_005228.4:c.2356G>A (EGFR)	NP_005219.2:p.Val786Met
NM_005228.5:c.2356G>A (EGFR) MANE Select	NP_005219.2:p.Val786Met
NM_001346897.2:c.2221G>A (EGFR)	NP_001333826.1:p.Val741Met
NM_001346898.2:c.2356G>A (EGFR)	NP_001333827.1:p.Val786Met
NM_001346900.2:c.2197G>A (EGFR)	NP_001333829.1:p.Val733Met
NM_001346941.2:c.1555G>A (EGFR)	NP_001333870.1:p.Val519Met
NM_001346899.2:c.2221G>A (EGFR)	NP_001333828.1:p.Val741Met