Canonical Allele Identifier: CA367577643
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs1396651256
gnomAD v2: 7-55221731-A-C
gnomAD v4: 7-55154038-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55154038A>C , CM000669.2:g.55154038A>C GRCh38
NC_000007.13:g.55221731A>C , CM000669.1:g.55221731A>C GRCh37
NC_000007.12:g.55189225A>C NCBI36
NG_007726.3:g.140007A>C , LRG_304:g.140007A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.616A>C ENSP00000413354.2:p.Thr206Pro
ENST00000700144.1:n.965A>C
ENST00000344576.7:c.775A>C ENSP00000345973.2:p.Thr259Pro
ENST00000275493.7:c.775A>C MANE Select ENSP00000275493.2:p.Thr259Pro
ENST00000275493.6:c.775A>C ENSP00000275493.2:p.Thr259Pro
ENST00000342916.7:c.775A>C ENSP00000342376.3:p.Thr259Pro
ENST00000344576.6:c.775A>C ENSP00000345973.2:p.Thr259Pro
ENST00000420316.6:c.775A>C ENSP00000413843.2:p.Thr259Pro
ENST00000442591.5:c.775A>C ENSP00000410031.1:p.Thr259Pro
ENST00000454757.6:c.640A>C ENSP00000395243.3:p.Thr214Pro
ENST00000455089.5:c.640A>C ENSP00000415559.1:p.Thr214Pro
NM_005228.3:c.775A>C , LRG_304t1:c.775A>C NP_005219.2:p.Thr259Pro
NM_201282.1:c.775A>C NP_958439.1:p.Thr259Pro
NM_201283.1:c.775A>C NP_958440.1:p.Thr259Pro
NM_201284.1:c.775A>C NP_958441.1:p.Thr259Pro
NM_001346897.1:c.640A>C NP_001333826.1:p.Thr214Pro
NM_001346898.1:c.775A>C NP_001333827.1:p.Thr259Pro
NM_001346899.1:c.640A>C NP_001333828.1:p.Thr214Pro
NM_001346900.1:c.616A>C NP_001333829.1:p.Thr206Pro
NM_001346941.1:c.89-1792A>C NP_001333870.1:n.89-1792A>C
NM_005228.4:c.775A>C NP_005219.2:p.Thr259Pro
NM_005228.5:c.775A>C MANE Select NP_005219.2:p.Thr259Pro
NM_001346897.2:c.640A>C NP_001333826.1:p.Thr214Pro
NM_001346898.2:c.775A>C NP_001333827.1:p.Thr259Pro
NM_001346900.2:c.616A>C NP_001333829.1:p.Thr206Pro
NM_001346941.2:c.89-1792A>C NP_001333870.1:n.89-1792A>C
NM_201282.2:c.775A>C NP_958439.1:p.Thr259Pro
NM_201284.2:c.775A>C NP_958441.1:p.Thr259Pro
NM_001346899.2:c.640A>C NP_001333828.1:p.Thr214Pro
NM_201283.2:c.775A>C NP_958440.1:p.Thr259Pro