Canonical Allele Identifier: CA1708928416
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55201217T= , CM000669.2:g.55201217T= GRCh38
NC_000007.13:g.55268910T= , CM000669.1:g.55268910T= GRCh37
NC_000007.12:g.55236404T= NCBI36
NG_007726.3:g.187186T= , LRG_304:g.187186T=

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2817T= ENSP00000413354.2:p.Pro939=
ENST00000700145.1:c.900-4130T=
ENST00000700146.1:n.720T=
ENST00000700147.1:n.645T=
ENST00000275493.7:c.2976T= MANE Select ENSP00000275493.2:p.Pro992=
ENST00000275493.6:c.2976T= ENSP00000275493.2:p.Pro992=
ENST00000442591.5:c.*28+28289T= ENSP00000410031.1:n.*28+28289T=
ENST00000454757.6:c.2841T= ENSP00000395243.3:p.Pro947=
ENST00000455089.5:c.2841T= ENSP00000415559.1:p.Pro947=
NM_005228.3:c.2976T= , LRG_304t1:c.2976T= NP_005219.2:p.Pro992=
NM_001346897.1:c.2841T= NP_001333826.1:p.Pro947=
NM_001346898.1:c.2976T= NP_001333827.1:p.Pro992=
NM_001346899.1:c.2841T= NP_001333828.1:p.Pro947=
NM_001346900.1:c.2817T= NP_001333829.1:p.Pro939=
NM_001346941.1:c.2175T= NP_001333870.1:p.Pro725=
NM_005228.4:c.2976T= NP_005219.2:p.Pro992=
NM_005228.5:c.2976T= MANE Select NP_005219.2:p.Pro992=
NM_001346897.2:c.2841T= NP_001333826.1:p.Pro947=
NM_001346898.2:c.2976T= NP_001333827.1:p.Pro992=
NM_001346900.2:c.2817T= NP_001333829.1:p.Pro939=
NM_001346941.2:c.2175T= NP_001333870.1:p.Pro725=
NM_001346899.2:c.2841T= NP_001333828.1:p.Pro947=