Canonical Allele Identifier: CA367584189

Gene: EGFR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174794C>G , CM000669.2:g.55174794C>G	GRCh38
NC_000007.13:g.55242487C>G , CM000669.1:g.55242487C>G	GRCh37
NC_000007.12:g.55209981C>G	NCBI36
NG_007726.3:g.160763C>G , LRG_304:g.160763C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2098C>G	ENSP00000413354.2:p.Pro700Ala
ENST00000700145.1:c.606C>G
ENST00000275493.7:c.2257C>G MANE Select	ENSP00000275493.2:p.Pro753Ala
ENST00000275493.6:c.2257C>G	ENSP00000275493.2:p.Pro753Ala
ENST00000442591.5:c.*28+1866C>G	ENSP00000410031.1:n.*28+1866C>G
ENST00000454757.6:c.2122C>G	ENSP00000395243.3:p.Pro708Ala
ENST00000455089.5:c.2122C>G	ENSP00000415559.1:p.Pro708Ala
NM_005228.3:c.2257C>G , LRG_304t1:c.2257C>G	NP_005219.2:p.Pro753Ala
NM_001346897.1:c.2122C>G	NP_001333826.1:p.Pro708Ala
NM_001346898.1:c.2257C>G	NP_001333827.1:p.Pro753Ala
NM_001346899.1:c.2122C>G	NP_001333828.1:p.Pro708Ala
NM_001346900.1:c.2098C>G	NP_001333829.1:p.Pro700Ala
NM_001346941.1:c.1456C>G	NP_001333870.1:p.Pro486Ala
NM_005228.4:c.2257C>G	NP_005219.2:p.Pro753Ala
NM_005228.5:c.2257C>G MANE Select	NP_005219.2:p.Pro753Ala
NM_001346897.2:c.2122C>G	NP_001333826.1:p.Pro708Ala
NM_001346898.2:c.2257C>G	NP_001333827.1:p.Pro753Ala
NM_001346900.2:c.2098C>G	NP_001333829.1:p.Pro700Ala
NM_001346941.2:c.1456C>G	NP_001333870.1:p.Pro486Ala
NM_001346899.2:c.2122C>G	NP_001333828.1:p.Pro708Ala