Canonical Allele Identifier: CA2714545531
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs1314666476

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55201105G>T , CM000669.2:g.55201105G>T GRCh38
NC_000007.13:g.55268798G>T , CM000669.1:g.55268798G>T GRCh37
NC_000007.12:g.55236292G>T NCBI36
NG_007726.3:g.187074G>T , LRG_304:g.187074G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2788-83G>T ENSP00000413354.2:n.2788-83G>T
ENST00000700145.1:c.900-4242G>T
ENST00000700146.1:n.691-83G>T
ENST00000700147.1:n.533G>T
ENST00000275493.7:c.2947-83G>T MANE Select ENSP00000275493.2:n.2947-83G>T
ENST00000275493.6:c.2947-83G>T ENSP00000275493.2:n.2947-83G>T
ENST00000442591.5:c.*28+28177G>T ENSP00000410031.1:n.*28+28177G>T
ENST00000454757.6:c.2812-83G>T ENSP00000395243.3:n.2812-83G>T
ENST00000455089.5:c.2812-83G>T ENSP00000415559.1:n.2812-83G>T
NM_005228.3:c.2947-83G>T , LRG_304t1:c.2947-83G>T NP_005219.2:n.2947-83G>T
NM_001346897.1:c.2812-83G>T NP_001333826.1:n.2812-83G>T
NM_001346898.1:c.2947-83G>T NP_001333827.1:n.2947-83G>T
NM_001346899.1:c.2812-83G>T NP_001333828.1:n.2812-83G>T
NM_001346900.1:c.2788-83G>T NP_001333829.1:n.2788-83G>T
NM_001346941.1:c.2146-83G>T NP_001333870.1:n.2146-83G>T
NM_005228.4:c.2947-83G>T NP_005219.2:n.2947-83G>T
NM_005228.5:c.2947-83G>T MANE Select NP_005219.2:n.2947-83G>T
NM_001346897.2:c.2812-83G>T NP_001333826.1:n.2812-83G>T
NM_001346898.2:c.2947-83G>T NP_001333827.1:n.2947-83G>T
NM_001346900.2:c.2788-83G>T NP_001333829.1:n.2788-83G>T
NM_001346941.2:c.2146-83G>T NP_001333870.1:n.2146-83G>T
NM_001346899.2:c.2812-83G>T NP_001333828.1:n.2812-83G>T