Canonical Allele Identifier: CA367580291
Gene: EGFR HGNC NCBI

Linked Data

COSMIC: COSM24848

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55191830C>G , CM000669.2:g.55191830C>G GRCh38
NC_000007.13:g.55259523C>G , CM000669.1:g.55259523C>G GRCh37
NC_000007.12:g.55227017C>G NCBI36
NG_007726.3:g.177799C>G , LRG_304:g.177799C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.2581C>G MANE Select ENSP00000275493.2:p.Leu861Val
ENST00000275493.6:c.2581C>G ENSP00000275493.2:p.Leu861Val
ENST00000442591.5:c.*28+18902C>G ENSP00000410031.1:n.*28+18902C>G
ENST00000454757.6:c.2446C>G ENSP00000395243.3:p.Leu816Val
ENST00000455089.5:c.2446C>G ENSP00000415559.1:p.Leu816Val
NM_005228.3:c.2581C>G , LRG_304t1:c.2581C>G NP_005219.2:p.Leu861Val
NM_001346897.1:c.2446C>G NP_001333826.1:p.Leu816Val
NM_001346898.1:c.2581C>G NP_001333827.1:p.Leu861Val
NM_001346899.1:c.2446C>G NP_001333828.1:p.Leu816Val
NM_001346900.1:c.2422C>G NP_001333829.1:p.Leu808Val
NM_001346941.1:c.1780C>G NP_001333870.1:p.Leu594Val
NM_005228.4:c.2581C>G NP_005219.2:p.Leu861Val
NM_005228.5:c.2581C>G MANE Select NP_005219.2:p.Leu861Val
NM_001346897.2:c.2446C>G NP_001333826.1:p.Leu816Val
NM_001346898.2:c.2581C>G NP_001333827.1:p.Leu861Val
NM_001346900.2:c.2422C>G NP_001333829.1:p.Leu808Val
NM_001346941.2:c.1780C>G NP_001333870.1:p.Leu594Val
NM_001346899.2:c.2446C>G NP_001333828.1:p.Leu816Val