Canonical Allele Identifier: CA1708922568
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55191792C= , CM000669.2:g.55191792C= GRCh38
NC_000007.13:g.55259485C= , CM000669.1:g.55259485C= GRCh37
NC_000007.12:g.55226979C= NCBI36
NG_007726.3:g.177761C= , LRG_304:g.177761C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000450046.2:c.2384C= ENSP00000413354.2:p.Pro795=
ENST00000700145.1:c.892C=
ENST00000275493.7:c.2543C= MANE Select ENSP00000275493.2:p.Pro848=
ENST00000275493.6:c.2543C= ENSP00000275493.2:p.Pro848=
ENST00000442591.5:c.*28+18864C= ENSP00000410031.1:n.*28+18864C=
ENST00000454757.6:c.2408C= ENSP00000395243.3:p.Pro803=
ENST00000455089.5:c.2408C= ENSP00000415559.1:p.Pro803=
NM_005228.3:c.2543C= , LRG_304t1:c.2543C= NP_005219.2:p.Pro848=
NM_001346897.1:c.2408C= NP_001333826.1:p.Pro803=
NM_001346898.1:c.2543C= NP_001333827.1:p.Pro848=
NM_001346899.1:c.2408C= NP_001333828.1:p.Pro803=
NM_001346900.1:c.2384C= NP_001333829.1:p.Pro795=
NM_001346941.1:c.1742C= NP_001333870.1:p.Pro581=
NM_005228.4:c.2543C= NP_005219.2:p.Pro848=
NM_005228.5:c.2543C= MANE Select NP_005219.2:p.Pro848=
NM_001346897.2:c.2408C= NP_001333826.1:p.Pro803=
NM_001346898.2:c.2543C= NP_001333827.1:p.Pro848=
NM_001346900.2:c.2384C= NP_001333829.1:p.Pro795=
NM_001346941.2:c.1742C= NP_001333870.1:p.Pro581=
NM_001346899.2:c.2408C= NP_001333828.1:p.Pro803=