Canonical Allele Identifier: CA454963455
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs2128932580
MyVariant Identifiers: chr7:g.55219030T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55151337T>A , CM000669.2:g.55151337T>A GRCh38
NC_000007.13:g.55219030T>A , CM000669.1:g.55219030T>A GRCh37
NC_000007.12:g.55186524T>A NCBI36
NG_007726.3:g.137306T>A , LRG_304:g.137306T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000450046.2:c.444T>A ENSP00000413354.2:p.Gly148=
ENST00000700144.1:n.793T>A
ENST00000344576.7:c.603T>A ENSP00000345973.2:p.Gly201=
ENST00000275493.7:c.603T>A MANE Select ENSP00000275493.2:p.Gly201=
ENST00000275493.6:c.603T>A ENSP00000275493.2:p.Gly201=
ENST00000342916.7:c.603T>A ENSP00000342376.3:p.Gly201=
ENST00000344576.6:c.603T>A ENSP00000345973.2:p.Gly201=
ENST00000420316.6:c.603T>A ENSP00000413843.2:p.Gly201=
ENST00000442591.5:c.603T>A ENSP00000410031.1:p.Gly201=
ENST00000454757.6:c.468T>A ENSP00000395243.3:p.Gly156=
ENST00000455089.5:c.468T>A ENSP00000415559.1:p.Gly156=
NM_005228.3:c.603T>A , LRG_304t1:c.603T>A NP_005219.2:p.Gly201=
NM_201282.1:c.603T>A NP_958439.1:p.Gly201=
NM_201283.1:c.603T>A NP_958440.1:p.Gly201=
NM_201284.1:c.603T>A NP_958441.1:p.Gly201=
NM_001346897.1:c.468T>A NP_001333826.1:p.Gly156=
NM_001346898.1:c.603T>A NP_001333827.1:p.Gly201=
NM_001346899.1:c.468T>A NP_001333828.1:p.Gly156=
NM_001346900.1:c.444T>A NP_001333829.1:p.Gly148=
NM_001346941.1:c.89-4493T>A NP_001333870.1:n.89-4493T>A
NM_005228.4:c.603T>A NP_005219.2:p.Gly201=
NM_005228.5:c.603T>A MANE Select NP_005219.2:p.Gly201=
NM_001346897.2:c.468T>A NP_001333826.1:p.Gly156=
NM_001346898.2:c.603T>A NP_001333827.1:p.Gly201=
NM_001346900.2:c.444T>A NP_001333829.1:p.Gly148=
NM_001346941.2:c.89-4493T>A NP_001333870.1:n.89-4493T>A
NM_201282.2:c.603T>A NP_958439.1:p.Gly201=
NM_201284.2:c.603T>A NP_958441.1:p.Gly201=
NM_001346899.2:c.468T>A NP_001333828.1:p.Gly156=
NM_201283.2:c.603T>A NP_958440.1:p.Gly201=