Canonical Allele Identifier: CA367580089
Gene: EGFR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55191731T>A , CM000669.2:g.55191731T>A GRCh38
NC_000007.13:g.55259424T>A , CM000669.1:g.55259424T>A GRCh37
NC_000007.12:g.55226918T>A NCBI36
NG_007726.3:g.177700T>A , LRG_304:g.177700T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.2482T>A MANE Select ENSP00000275493.2:p.Leu828Met
ENST00000275493.6:c.2482T>A ENSP00000275493.2:p.Leu828Met
ENST00000442591.5:c.*28+18803T>A ENSP00000410031.1:n.*28+18803T>A
ENST00000454757.6:c.2347T>A ENSP00000395243.3:p.Leu783Met
ENST00000455089.5:c.2347T>A ENSP00000415559.1:p.Leu783Met
NM_005228.3:c.2482T>A , LRG_304t1:c.2482T>A NP_005219.2:p.Leu828Met
NM_001346897.1:c.2347T>A NP_001333826.1:p.Leu783Met
NM_001346898.1:c.2482T>A NP_001333827.1:p.Leu828Met
NM_001346899.1:c.2347T>A NP_001333828.1:p.Leu783Met
NM_001346900.1:c.2323T>A NP_001333829.1:p.Leu775Met
NM_001346941.1:c.1681T>A NP_001333870.1:p.Leu561Met
NM_005228.4:c.2482T>A NP_005219.2:p.Leu828Met
NM_005228.5:c.2482T>A MANE Select NP_005219.2:p.Leu828Met
NM_001346897.2:c.2347T>A NP_001333826.1:p.Leu783Met
NM_001346898.2:c.2482T>A NP_001333827.1:p.Leu828Met
NM_001346900.2:c.2323T>A NP_001333829.1:p.Leu775Met
NM_001346941.2:c.1681T>A NP_001333870.1:p.Leu561Met
NM_001346899.2:c.2347T>A NP_001333828.1:p.Leu783Met