Canonical Allele Identifier: CA367578660
Gene: EGFR HGNC NCBI
EGFR-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1584238358

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