Canonical Allele Identifier: CA367578660

Gene: EGFR EGFR-AS1

Linked Data

• dbSNP Id: rs1584238358
• MyVariant Identifiers: chr7:g.55249014A>C (hg19) ; chr7:g.55181321A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181321A>C , CM000669.2:g.55181321A>C	GRCh38
NC_000007.13:g.55249014A>C , CM000669.1:g.55249014A>C	GRCh37
NC_000007.12:g.55216508A>C	NCBI36
NG_007726.3:g.167290A>C , LRG_304:g.167290A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2153A>C (EGFR)	ENSP00000413354.2:p.Asn718Thr
ENST00000700145.1:c.661A>C (EGFR)
ENST00000275493.7:c.2312A>C (EGFR) MANE Select	ENSP00000275493.2:p.Asn771Thr
ENST00000275493.6:c.2312A>C (EGFR)	ENSP00000275493.2:p.Asn771Thr
ENST00000442591.5:c.*28+8393A>C (EGFR)	ENSP00000410031.1:n.*28+8393A>C
ENST00000454757.6:c.2177A>C (EGFR)	ENSP00000395243.3:p.Asn726Thr
ENST00000455089.5:c.2177A>C (EGFR)	ENSP00000415559.1:p.Asn726Thr
NM_005228.3:c.2312A>C , LRG_304t1:c.2312A>C (EGFR)	NP_005219.2:p.Asn771Thr
NR_047551.1:n.1250T>G (EGFR-AS1)
NM_001346897.1:c.2177A>C (EGFR)	NP_001333826.1:p.Asn726Thr
NM_001346898.1:c.2312A>C (EGFR)	NP_001333827.1:p.Asn771Thr
NM_001346899.1:c.2177A>C (EGFR)	NP_001333828.1:p.Asn726Thr
NM_001346900.1:c.2153A>C (EGFR)	NP_001333829.1:p.Asn718Thr
NM_001346941.1:c.1511A>C (EGFR)	NP_001333870.1:p.Asn504Thr
NM_005228.4:c.2312A>C (EGFR)	NP_005219.2:p.Asn771Thr
NM_005228.5:c.2312A>C (EGFR) MANE Select	NP_005219.2:p.Asn771Thr
NM_001346897.2:c.2177A>C (EGFR)	NP_001333826.1:p.Asn726Thr
NM_001346898.2:c.2312A>C (EGFR)	NP_001333827.1:p.Asn771Thr
NM_001346900.2:c.2153A>C (EGFR)	NP_001333829.1:p.Asn718Thr
NM_001346941.2:c.1511A>C (EGFR)	NP_001333870.1:p.Asn504Thr
NM_001346899.2:c.2177A>C (EGFR)	NP_001333828.1:p.Asn726Thr