Canonical Allele Identifier: CA454965708

Gene: EGFR

Linked Data

• dbSNP Id: rs142569931
• MyVariant Identifiers: chr7:g.55221730C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55154037C>G , CM000669.2:g.55154037C>G	GRCh38
NC_000007.13:g.55221730C>G , CM000669.1:g.55221730C>G	GRCh37
NC_000007.12:g.55189224C>G	NCBI36
NG_007726.3:g.140006C>G , LRG_304:g.140006C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.615C>G	ENSP00000413354.2:p.Ala205=
ENST00000700144.1:n.964C>G
ENST00000344576.7:c.774C>G	ENSP00000345973.2:p.Ala258=
ENST00000275493.7:c.774C>G MANE Select	ENSP00000275493.2:p.Ala258=
ENST00000275493.6:c.774C>G	ENSP00000275493.2:p.Ala258=
ENST00000342916.7:c.774C>G	ENSP00000342376.3:p.Ala258=
ENST00000344576.6:c.774C>G	ENSP00000345973.2:p.Ala258=
ENST00000420316.6:c.774C>G	ENSP00000413843.2:p.Ala258=
ENST00000442591.5:c.774C>G	ENSP00000410031.1:p.Ala258=
ENST00000454757.6:c.639C>G	ENSP00000395243.3:p.Ala213=
ENST00000455089.5:c.639C>G	ENSP00000415559.1:p.Ala213=
NM_005228.3:c.774C>G , LRG_304t1:c.774C>G	NP_005219.2:p.Ala258=
NM_201282.1:c.774C>G	NP_958439.1:p.Ala258=
NM_201283.1:c.774C>G	NP_958440.1:p.Ala258=
NM_201284.1:c.774C>G	NP_958441.1:p.Ala258=
NM_001346897.1:c.639C>G	NP_001333826.1:p.Ala213=
NM_001346898.1:c.774C>G	NP_001333827.1:p.Ala258=
NM_001346899.1:c.639C>G	NP_001333828.1:p.Ala213=
NM_001346900.1:c.615C>G	NP_001333829.1:p.Ala205=
NM_001346941.1:c.89-1793C>G	NP_001333870.1:n.89-1793C>G
NM_005228.4:c.774C>G	NP_005219.2:p.Ala258=
NM_005228.5:c.774C>G MANE Select	NP_005219.2:p.Ala258=
NM_001346897.2:c.639C>G	NP_001333826.1:p.Ala213=
NM_001346898.2:c.774C>G	NP_001333827.1:p.Ala258=
NM_001346900.2:c.615C>G	NP_001333829.1:p.Ala205=
NM_001346941.2:c.89-1793C>G	NP_001333870.1:n.89-1793C>G
NM_201282.2:c.774C>G	NP_958439.1:p.Ala258=
NM_201284.2:c.774C>G	NP_958441.1:p.Ala258=
NM_001346899.2:c.639C>G	NP_001333828.1:p.Ala213=
NM_201283.2:c.774C>G	NP_958440.1:p.Ala258=