Canonical Allele Identifier: CA367580310
Gene: EGFR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55191842G>T , CM000669.2:g.55191842G>T GRCh38
NC_000007.13:g.55259535G>T , CM000669.1:g.55259535G>T GRCh37
NC_000007.12:g.55227029G>T NCBI36
NG_007726.3:g.177811G>T , LRG_304:g.177811G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2434G>T ENSP00000413354.2:p.Glu812Ter
ENST00000700145.1:c.899+43G>T
ENST00000275493.7:c.2593G>T MANE Select ENSP00000275493.2:p.Glu865Ter
ENST00000275493.6:c.2593G>T ENSP00000275493.2:p.Glu865Ter
ENST00000442591.5:c.*28+18914G>T ENSP00000410031.1:n.*28+18914G>T
ENST00000454757.6:c.2458G>T ENSP00000395243.3:p.Glu820Ter
ENST00000455089.5:c.2458G>T ENSP00000415559.1:p.Glu820Ter
NM_005228.3:c.2593G>T , LRG_304t1:c.2593G>T NP_005219.2:p.Glu865Ter
NM_001346897.1:c.2458G>T NP_001333826.1:p.Glu820Ter
NM_001346898.1:c.2593G>T NP_001333827.1:p.Glu865Ter
NM_001346899.1:c.2458G>T NP_001333828.1:p.Glu820Ter
NM_001346900.1:c.2434G>T NP_001333829.1:p.Glu812Ter
NM_001346941.1:c.1792G>T NP_001333870.1:p.Glu598Ter
NM_005228.4:c.2593G>T NP_005219.2:p.Glu865Ter
NM_005228.5:c.2593G>T MANE Select NP_005219.2:p.Glu865Ter
NM_001346897.2:c.2458G>T NP_001333826.1:p.Glu820Ter
NM_001346898.2:c.2593G>T NP_001333827.1:p.Glu865Ter
NM_001346900.2:c.2434G>T NP_001333829.1:p.Glu812Ter
NM_001346941.2:c.1792G>T NP_001333870.1:p.Glu598Ter
NM_001346899.2:c.2458G>T NP_001333828.1:p.Glu820Ter