Canonical Allele Identifier: CA12539703
Gene: EGFR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12535536

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55086688G>A , CM000669.2:g.55086688G>A GRCh38
NC_000007.13:g.55154381G>A , CM000669.1:g.55154381G>A GRCh37
NC_000007.12:g.55121875G>A NCBI36
NG_007726.3:g.72657G>A , LRG_304:g.72657G>A

Transcript Alleles

HGVS Amino-acid change
NM_005228.3:c.89-55598G>A , LRG_304t1:c.89-55598G>A NP_005219.2:p.=
NM_201282.1:c.89-55598G>A VV NP_958439.1:p.=
NM_201283.1:c.89-55598G>A VV NP_958440.1:p.=
NM_201284.1:c.89-55598G>A VV NP_958441.1:p.=
NM_001346897.1:c.89-55598G>A VV NP_001333826.1:p.=
NM_001346898.1:c.89-55598G>A VV NP_001333827.1:p.=
NM_001346899.1:c.89-55598G>A VV NP_001333828.1:p.=
NM_001346941.1:c.88+67323G>A VV NP_001333870.1:p.=
NM_005228.4:c.89-55598G>A VV NP_005219.2:p.=
NM_005228.5:c.89-55598G>A VV MANE Preferred NP_005219.2:p.=
ENST00000275493.6:c.89-55598G>A ENSP00000275493.2:p.=
ENST00000342916.7:c.89-55598G>A ENSP00000342376.3:p.=
ENST00000344576.6:c.89-55598G>A ENSP00000345973.2:p.=
ENST00000420316.6:c.89-55598G>A ENSP00000413843.2:p.=
ENST00000442591.5:c.89-55598G>A ENSP00000410031.1:p.=
ENST00000454757.6:c.89-55598G>A ENSP00000395243.3:p.=
ENST00000455089.5:c.89-55598G>A ENSP00000415559.1:p.=
ENST00000463948.1:n.216-32368G>A