Canonical Allele Identifier: CA367577864
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs150549265

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55154137G>T , CM000669.2:g.55154137G>T GRCh38
NC_000007.13:g.55221830G>T , CM000669.1:g.55221830G>T GRCh37
NC_000007.12:g.55189324G>T NCBI36
NG_007726.3:g.140106G>T , LRG_304:g.140106G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.715G>T ENSP00000413354.2:p.Val239Leu
ENST00000700144.1:n.1064G>T
ENST00000344576.7:c.874G>T ENSP00000345973.2:p.Val292Leu
ENST00000275493.7:c.874G>T MANE Select ENSP00000275493.2:p.Val292Leu
ENST00000275493.6:c.874G>T ENSP00000275493.2:p.Val292Leu
ENST00000342916.7:c.874G>T ENSP00000342376.3:p.Val292Leu
ENST00000344576.6:c.874G>T ENSP00000345973.2:p.Val292Leu
ENST00000420316.6:c.874G>T ENSP00000413843.2:p.Val292Leu
ENST00000442591.5:c.874G>T ENSP00000410031.1:p.Val292Leu
ENST00000454757.6:c.739G>T ENSP00000395243.3:p.Val247Leu
ENST00000455089.5:c.739G>T ENSP00000415559.1:p.Val247Leu
NM_005228.3:c.874G>T , LRG_304t1:c.874G>T NP_005219.2:p.Val292Leu
NM_201282.1:c.874G>T NP_958439.1:p.Val292Leu
NM_201283.1:c.874G>T NP_958440.1:p.Val292Leu
NM_201284.1:c.874G>T NP_958441.1:p.Val292Leu
NM_001346897.1:c.739G>T NP_001333826.1:p.Val247Leu
NM_001346898.1:c.874G>T NP_001333827.1:p.Val292Leu
NM_001346899.1:c.739G>T NP_001333828.1:p.Val247Leu
NM_001346900.1:c.715G>T NP_001333829.1:p.Val239Leu
NM_001346941.1:c.89-1693G>T NP_001333870.1:n.89-1693G>T
NM_005228.4:c.874G>T NP_005219.2:p.Val292Leu
NM_005228.5:c.874G>T MANE Select NP_005219.2:p.Val292Leu
NM_001346897.2:c.739G>T NP_001333826.1:p.Val247Leu
NM_001346898.2:c.874G>T NP_001333827.1:p.Val292Leu
NM_001346900.2:c.715G>T NP_001333829.1:p.Val239Leu
NM_001346941.2:c.89-1693G>T NP_001333870.1:n.89-1693G>T
NM_201282.2:c.874G>T NP_958439.1:p.Val292Leu
NM_201284.2:c.874G>T NP_958441.1:p.Val292Leu
NM_001346899.2:c.739G>T NP_001333828.1:p.Val247Leu
NM_201283.2:c.874G>T NP_958440.1:p.Val292Leu