Canonical Allele Identifier: CA15525638
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs12718945

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55125270T>G , CM000669.2:g.55125270T>G GRCh38
NC_000007.13:g.55192963T>G , CM000669.1:g.55192963T>G GRCh37
NC_000007.12:g.55160457T>G NCBI36
NG_007726.3:g.111239T>G , LRG_304:g.111239T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.89-17016T>G MANE Select ENSP00000275493.2:p.=
ENST00000275493.6:c.89-17016T>G ENSP00000275493.2:p.=
ENST00000342916.7:c.89-17016T>G ENSP00000342376.3:p.=
ENST00000344576.6:c.89-17016T>G ENSP00000345973.2:p.=
ENST00000420316.6:c.89-17016T>G ENSP00000413843.2:p.=
ENST00000442591.5:c.89-17016T>G ENSP00000410031.1:p.=
ENST00000450046.1:c.-72+15312T>G ENSP00000413354.1:p.=
ENST00000454757.6:c.89-17016T>G ENSP00000395243.3:p.=
ENST00000455089.5:c.89-17016T>G ENSP00000415559.1:p.=
NM_005228.3:c.89-17016T>G , LRG_304t1:c.89-17016T>G NP_005219.2:p.=
NM_201282.1:c.89-17016T>G NP_958439.1:p.=
NM_201283.1:c.89-17016T>G NP_958440.1:p.=
NM_201284.1:c.89-17016T>G NP_958441.1:p.=
NM_001346897.1:c.89-17016T>G NP_001333826.1:p.=
NM_001346898.1:c.89-17016T>G NP_001333827.1:p.=
NM_001346899.1:c.89-17016T>G NP_001333828.1:p.=
NM_001346900.1:c.-72+15312T>G NP_001333829.1:p.=
NM_001346941.1:c.89-30560T>G NP_001333870.1:p.=
NM_005228.4:c.89-17016T>G NP_005219.2:p.=
NM_005228.5:c.89-17016T>G MANE Select NP_005219.2:p.=
NM_001346897.2:c.89-17016T>G NP_001333826.1:p.=
NM_001346898.2:c.89-17016T>G NP_001333827.1:p.=
NM_001346900.2:c.-72+15312T>G NP_001333829.1:p.=
NM_001346941.2:c.89-30560T>G NP_001333870.1:p.=
NM_201282.2:c.89-17016T>G NP_958439.1:p.=
NM_201284.2:c.89-17016T>G NP_958441.1:p.=
NM_001346899.2:c.89-17016T>G NP_001333828.1:p.=
NM_201283.2:c.89-17016T>G NP_958440.1:p.=