Canonical Allele Identifier: CA4266122

Gene: EGFR

Linked Data

• dbSNP Id: rs372812795
• ExAC: 7:55259604 G / A
• gnomAD v2: 7-55259604-G-A
• gnomAD v3: 7-55191911-G-A
• gnomAD v4: 7-55191911-G-A
• MyVariant Identifiers: chr7:g.55259604G>A (hg19) ; chr7:g.55191911G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191911G>A , CM000669.2:g.55191911G>A	GRCh38
NC_000007.13:g.55259604G>A , CM000669.1:g.55259604G>A	GRCh37
NC_000007.12:g.55227098G>A	NCBI36
NG_007726.3:g.177880G>A , LRG_304:g.177880G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2466+37G>A	ENSP00000413354.2:n.2466+37G>A
ENST00000700145.1:c.899+112G>A
ENST00000275493.7:c.2625+37G>A MANE Select	ENSP00000275493.2:n.2625+37G>A
ENST00000275493.6:c.2625+37G>A	ENSP00000275493.2:n.2625+37G>A
ENST00000442591.5:c.*28+18983G>A	ENSP00000410031.1:n.*28+18983G>A
ENST00000454757.6:c.2490+37G>A	ENSP00000395243.3:n.2490+37G>A
ENST00000455089.5:c.2490+37G>A	ENSP00000415559.1:n.2490+37G>A
NM_005228.3:c.2625+37G>A , LRG_304t1:c.2625+37G>A	NP_005219.2:n.2625+37G>A
NM_001346897.1:c.2490+37G>A	NP_001333826.1:n.2490+37G>A
NM_001346898.1:c.2625+37G>A	NP_001333827.1:n.2625+37G>A
NM_001346899.1:c.2490+37G>A	NP_001333828.1:n.2490+37G>A
NM_001346900.1:c.2466+37G>A	NP_001333829.1:n.2466+37G>A
NM_001346941.1:c.1824+37G>A	NP_001333870.1:n.1824+37G>A
NM_005228.4:c.2625+37G>A	NP_005219.2:n.2625+37G>A
NM_005228.5:c.2625+37G>A MANE Select	NP_005219.2:n.2625+37G>A
NM_001346897.2:c.2490+37G>A	NP_001333826.1:n.2490+37G>A
NM_001346898.2:c.2625+37G>A	NP_001333827.1:n.2625+37G>A
NM_001346900.2:c.2466+37G>A	NP_001333829.1:n.2466+37G>A
NM_001346941.2:c.1824+37G>A	NP_001333870.1:n.1824+37G>A
NM_001346899.2:c.2490+37G>A	NP_001333828.1:n.2490+37G>A