Canonical Allele Identifier: CA2682854691

Gene: EGFR

Linked Data

• gnomAD v4: 7-55174021-G-GCGGAGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174021_55174022insCGGAGGC , CM000669.2:g.55174021_55174022insCGGAGGC	GRCh38
NC_000007.13:g.55241714_55241715insCGGAGGC , CM000669.1:g.55241714_55241715insCGGAGGC	GRCh37
NC_000007.12:g.55209208_55209209insCGGAGGC	NCBI36
NG_007726.3:g.159990_159991insCGGAGGC , LRG_304:g.159990_159991insCGGAGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2003_2004insCGGAGGC	ENSP00000413354.2:p.Ala669GlyfsTer9
ENST00000700145.1:c.511_512insCGGAGGC
ENST00000275493.7:c.2162_2163insCGGAGGC MANE Select	ENSP00000275493.2:p.Ala722GlyfsTer9
ENST00000275493.6:c.2162_2163insCGGAGGC	ENSP00000275493.2:p.Ala722GlyfsTer9
ENST00000442591.5:c.*28+1093_*28+1094insCGGAGGC	ENSP00000410031.1:n.*28+1093_*28+1094insCGGAGGC
ENST00000454757.6:c.2027_2028insCGGAGGC	ENSP00000395243.3:p.Ala677GlyfsTer9
ENST00000455089.5:c.2027_2028insCGGAGGC	ENSP00000415559.1:p.Ala677GlyfsTer9
NM_005228.3:c.2162_2163insCGGAGGC , LRG_304t1:c.2162_2163insCGGAGGC	NP_005219.2:p.Ala722GlyfsTer9
NM_001346897.1:c.2027_2028insCGGAGGC	NP_001333826.1:p.Ala677GlyfsTer9
NM_001346898.1:c.2162_2163insCGGAGGC	NP_001333827.1:p.Ala722GlyfsTer9
NM_001346899.1:c.2027_2028insCGGAGGC	NP_001333828.1:p.Ala677GlyfsTer9
NM_001346900.1:c.2003_2004insCGGAGGC	NP_001333829.1:p.Ala669GlyfsTer9
NM_001346941.1:c.1361_1362insCGGAGGC	NP_001333870.1:p.Ala455GlyfsTer9
NM_005228.4:c.2162_2163insCGGAGGC	NP_005219.2:p.Ala722GlyfsTer9
NM_005228.5:c.2162_2163insCGGAGGC MANE Select	NP_005219.2:p.Ala722GlyfsTer9
NM_001346897.2:c.2027_2028insCGGAGGC	NP_001333826.1:p.Ala677GlyfsTer9
NM_001346898.2:c.2162_2163insCGGAGGC	NP_001333827.1:p.Ala722GlyfsTer9
NM_001346900.2:c.2003_2004insCGGAGGC	NP_001333829.1:p.Ala669GlyfsTer9
NM_001346941.2:c.1361_1362insCGGAGGC	NP_001333870.1:p.Ala455GlyfsTer9
NM_001346899.2:c.2027_2028insCGGAGGC	NP_001333828.1:p.Ala677GlyfsTer9