Canonical Allele Identifier: CA1708928414
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55201212A= , CM000669.2:g.55201212A= GRCh38
NC_000007.13:g.55268905A= , CM000669.1:g.55268905A= GRCh37
NC_000007.12:g.55236399A= NCBI36
NG_007726.3:g.187181A= , LRG_304:g.187181A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000450046.2:c.2812A= ENSP00000413354.2:p.Ser938=
ENST00000700145.1:c.900-4135A=
ENST00000700146.1:n.715A=
ENST00000700147.1:n.640A=
ENST00000275493.7:c.2971A= MANE Select ENSP00000275493.2:p.Ser991=
ENST00000275493.6:c.2971A= ENSP00000275493.2:p.Ser991=
ENST00000442591.5:c.*28+28284A= ENSP00000410031.1:n.*28+28284A=
ENST00000454757.6:c.2836A= ENSP00000395243.3:p.Ser946=
ENST00000455089.5:c.2836A= ENSP00000415559.1:p.Ser946=
NM_005228.3:c.2971A= , LRG_304t1:c.2971A= NP_005219.2:p.Ser991=
NM_001346897.1:c.2836A= NP_001333826.1:p.Ser946=
NM_001346898.1:c.2971A= NP_001333827.1:p.Ser991=
NM_001346899.1:c.2836A= NP_001333828.1:p.Ser946=
NM_001346900.1:c.2812A= NP_001333829.1:p.Ser938=
NM_001346941.1:c.2170A= NP_001333870.1:p.Ser724=
NM_005228.4:c.2971A= NP_005219.2:p.Ser991=
NM_005228.5:c.2971A= MANE Select NP_005219.2:p.Ser991=
NM_001346897.2:c.2836A= NP_001333826.1:p.Ser946=
NM_001346898.2:c.2971A= NP_001333827.1:p.Ser991=
NM_001346900.2:c.2812A= NP_001333829.1:p.Ser938=
NM_001346941.2:c.2170A= NP_001333870.1:p.Ser724=
NM_001346899.2:c.2836A= NP_001333828.1:p.Ser946=