Canonical Allele Identifier: CA1708905123
Gene: EGFR HGNC NCBI
EGFR-AS1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2147T= (EGFR) ENSP00000413354.2:p.Val716=
ENST00000700145.1:c.655T= (EGFR)
ENST00000275493.7:c.2306T= (EGFR) MANE Select ENSP00000275493.2:p.Val769=
ENST00000275493.6:c.2306T= (EGFR) ENSP00000275493.2:p.Val769=
ENST00000442591.5:c.*28+8387T= (EGFR) ENSP00000410031.1:n.*28+8387T=
ENST00000454757.6:c.2171T= (EGFR) ENSP00000395243.3:p.Val724=
ENST00000455089.5:c.2171T= (EGFR) ENSP00000415559.1:p.Val724=
NM_005228.3:c.2306T= , LRG_304t1:c.2306T= (EGFR) NP_005219.2:p.Val769=
NR_047551.1:n.1256A= (EGFR-AS1)
NM_001346897.1:c.2171T= (EGFR) NP_001333826.1:p.Val724=
NM_001346898.1:c.2306T= (EGFR) NP_001333827.1:p.Val769=
NM_001346899.1:c.2171T= (EGFR) NP_001333828.1:p.Val724=
NM_001346900.1:c.2147T= (EGFR) NP_001333829.1:p.Val716=
NM_001346941.1:c.1505T= (EGFR) NP_001333870.1:p.Val502=
NM_005228.4:c.2306T= (EGFR) NP_005219.2:p.Val769=
NM_005228.5:c.2306T= (EGFR) MANE Select NP_005219.2:p.Val769=
NM_001346897.2:c.2171T= (EGFR) NP_001333826.1:p.Val724=
NM_001346898.2:c.2306T= (EGFR) NP_001333827.1:p.Val769=
NM_001346900.2:c.2147T= (EGFR) NP_001333829.1:p.Val716=
NM_001346941.2:c.1505T= (EGFR) NP_001333870.1:p.Val502=
NM_001346899.2:c.2171T= (EGFR) NP_001333828.1:p.Val724=