Canonical Allele Identifier: CA1708928413
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55201209C= , CM000669.2:g.55201209C= GRCh38
NC_000007.13:g.55268902C= , CM000669.1:g.55268902C= GRCh37
NC_000007.12:g.55236396C= NCBI36
NG_007726.3:g.187178C= , LRG_304:g.187178C=

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2809C= ENSP00000413354.2:p.Pro937=
ENST00000700145.1:c.900-4138C=
ENST00000700146.1:n.712C=
ENST00000700147.1:n.637C=
ENST00000275493.7:c.2968C= MANE Select ENSP00000275493.2:p.Pro990=
ENST00000275493.6:c.2968C= ENSP00000275493.2:p.Pro990=
ENST00000442591.5:c.*28+28281C= ENSP00000410031.1:n.*28+28281C=
ENST00000454757.6:c.2833C= ENSP00000395243.3:p.Pro945=
ENST00000455089.5:c.2833C= ENSP00000415559.1:p.Pro945=
NM_005228.3:c.2968C= , LRG_304t1:c.2968C= NP_005219.2:p.Pro990=
NM_001346897.1:c.2833C= NP_001333826.1:p.Pro945=
NM_001346898.1:c.2968C= NP_001333827.1:p.Pro990=
NM_001346899.1:c.2833C= NP_001333828.1:p.Pro945=
NM_001346900.1:c.2809C= NP_001333829.1:p.Pro937=
NM_001346941.1:c.2167C= NP_001333870.1:p.Pro723=
NM_005228.4:c.2968C= NP_005219.2:p.Pro990=
NM_005228.5:c.2968C= MANE Select NP_005219.2:p.Pro990=
NM_001346897.2:c.2833C= NP_001333826.1:p.Pro945=
NM_001346898.2:c.2968C= NP_001333827.1:p.Pro990=
NM_001346900.2:c.2809C= NP_001333829.1:p.Pro937=
NM_001346941.2:c.2167C= NP_001333870.1:p.Pro723=
NM_001346899.2:c.2833C= NP_001333828.1:p.Pro945=