Canonical Allele Identifier: CA367578616

Gene: EGFR EGFR-AS1

Linked Data

• COSMIC: COSM3736992
• MyVariant Identifiers: chr7:g.55249008T>C (hg19) ; chr7:g.55181315T>C (hg38)
• CIViC: CA367578616

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181315T>C , CM000669.2:g.55181315T>C	GRCh38
NC_000007.13:g.55249008T>C , CM000669.1:g.55249008T>C	GRCh37
NC_000007.12:g.55216502T>C	NCBI36
NG_007726.3:g.167284T>C , LRG_304:g.167284T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2147T>C (EGFR)	ENSP00000413354.2:p.Val716Ala
ENST00000700145.1:c.655T>C (EGFR)
ENST00000275493.7:c.2306T>C (EGFR) MANE Select	ENSP00000275493.2:p.Val769Ala
ENST00000275493.6:c.2306T>C (EGFR)	ENSP00000275493.2:p.Val769Ala
ENST00000442591.5:c.*28+8387T>C (EGFR)	ENSP00000410031.1:n.*28+8387T>C
ENST00000454757.6:c.2171T>C (EGFR)	ENSP00000395243.3:p.Val724Ala
ENST00000455089.5:c.2171T>C (EGFR)	ENSP00000415559.1:p.Val724Ala
NM_005228.3:c.2306T>C , LRG_304t1:c.2306T>C (EGFR)	NP_005219.2:p.Val769Ala
NR_047551.1:n.1256A>G (EGFR-AS1)
NM_001346897.1:c.2171T>C (EGFR)	NP_001333826.1:p.Val724Ala
NM_001346898.1:c.2306T>C (EGFR)	NP_001333827.1:p.Val769Ala
NM_001346899.1:c.2171T>C (EGFR)	NP_001333828.1:p.Val724Ala
NM_001346900.1:c.2147T>C (EGFR)	NP_001333829.1:p.Val716Ala
NM_001346941.1:c.1505T>C (EGFR)	NP_001333870.1:p.Val502Ala
NM_005228.4:c.2306T>C (EGFR)	NP_005219.2:p.Val769Ala
NM_005228.5:c.2306T>C (EGFR) MANE Select	NP_005219.2:p.Val769Ala
NM_001346897.2:c.2171T>C (EGFR)	NP_001333826.1:p.Val724Ala
NM_001346898.2:c.2306T>C (EGFR)	NP_001333827.1:p.Val769Ala
NM_001346900.2:c.2147T>C (EGFR)	NP_001333829.1:p.Val716Ala
NM_001346941.2:c.1505T>C (EGFR)	NP_001333870.1:p.Val502Ala
NM_001346899.2:c.2171T>C (EGFR)	NP_001333828.1:p.Val724Ala