Canonical Allele Identifier: CA1708891248
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs1793457131

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55125288G>T , CM000669.2:g.55125288G>T GRCh38
NC_000007.13:g.55192981G>T , CM000669.1:g.55192981G>T GRCh37
NC_000007.12:g.55160475G>T NCBI36
NG_007726.3:g.111257G>T , LRG_304:g.111257G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.-72+15330G>T ENSP00000413354.2:n.-72+15330G>T
ENST00000700144.1:n.279-16998G>T
ENST00000344576.7:c.89-16998G>T ENSP00000345973.2:n.89-16998G>T
ENST00000275493.7:c.89-16998G>T MANE Select ENSP00000275493.2:n.89-16998G>T
ENST00000275493.6:c.89-16998G>T ENSP00000275493.2:n.89-16998G>T
ENST00000342916.7:c.89-16998G>T ENSP00000342376.3:n.89-16998G>T
ENST00000344576.6:c.89-16998G>T ENSP00000345973.2:n.89-16998G>T
ENST00000420316.6:c.89-16998G>T ENSP00000413843.2:n.89-16998G>T
ENST00000442591.5:c.89-16998G>T ENSP00000410031.1:n.89-16998G>T
ENST00000450046.1:c.-72+15330G>T ENSP00000413354.1:n.-72+15330G>T
ENST00000454757.6:c.89-16998G>T ENSP00000395243.3:n.89-16998G>T
ENST00000455089.5:c.89-16998G>T ENSP00000415559.1:n.89-16998G>T
NM_005228.3:c.89-16998G>T , LRG_304t1:c.89-16998G>T NP_005219.2:n.89-16998G>T
NM_201282.1:c.89-16998G>T NP_958439.1:n.89-16998G>T
NM_201283.1:c.89-16998G>T NP_958440.1:n.89-16998G>T
NM_201284.1:c.89-16998G>T NP_958441.1:n.89-16998G>T
NM_001346897.1:c.89-16998G>T NP_001333826.1:n.89-16998G>T
NM_001346898.1:c.89-16998G>T NP_001333827.1:n.89-16998G>T
NM_001346899.1:c.89-16998G>T NP_001333828.1:n.89-16998G>T
NM_001346900.1:c.-72+15330G>T NP_001333829.1:n.-72+15330G>T
NM_001346941.1:c.89-30542G>T NP_001333870.1:n.89-30542G>T
NM_005228.4:c.89-16998G>T NP_005219.2:n.89-16998G>T
NM_005228.5:c.89-16998G>T MANE Select NP_005219.2:n.89-16998G>T
NM_001346897.2:c.89-16998G>T NP_001333826.1:n.89-16998G>T
NM_001346898.2:c.89-16998G>T NP_001333827.1:n.89-16998G>T
NM_001346900.2:c.-72+15330G>T NP_001333829.1:n.-72+15330G>T
NM_001346941.2:c.89-30542G>T NP_001333870.1:n.89-30542G>T
NM_201282.2:c.89-16998G>T NP_958439.1:n.89-16998G>T
NM_201284.2:c.89-16998G>T NP_958441.1:n.89-16998G>T
NM_001346899.2:c.89-16998G>T NP_001333828.1:n.89-16998G>T
NM_201283.2:c.89-16998G>T NP_958440.1:n.89-16998G>T