Canonical Allele Identifier: CA2775498835

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174624_55174625insT , CM000669.2:g.55174624_55174625insT	GRCh38
NC_000007.13:g.55242317_55242318insT , CM000669.1:g.55242317_55242318insT	GRCh37
NC_000007.12:g.55209811_55209812insT	NCBI36
NG_007726.3:g.160593_160594insT , LRG_304:g.160593_160594insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2026-98_2026-97insT	ENSP00000413354.2:n.2026-98_2026-97insT
ENST00000700145.1:c.534-98_534-97insT
ENST00000275493.7:c.2185-98_2185-97insT MANE Select	ENSP00000275493.2:n.2185-98_2185-97insT
ENST00000275493.6:c.2185-98_2185-97insT	ENSP00000275493.2:n.2185-98_2185-97insT
ENST00000442591.5:c.*28+1696_*28+1697insT	ENSP00000410031.1:n.*28+1696_*28+1697insT
ENST00000454757.6:c.2050-98_2050-97insT	ENSP00000395243.3:n.2050-98_2050-97insT
ENST00000455089.5:c.2050-98_2050-97insT	ENSP00000415559.1:n.2050-98_2050-97insT
NM_005228.3:c.2185-98_2185-97insT , LRG_304t1:c.2185-98_2185-97insT	NP_005219.2:n.2185-98_2185-97insT
NM_001346897.1:c.2050-98_2050-97insT	NP_001333826.1:n.2050-98_2050-97insT
NM_001346898.1:c.2185-98_2185-97insT	NP_001333827.1:n.2185-98_2185-97insT
NM_001346899.1:c.2050-98_2050-97insT	NP_001333828.1:n.2050-98_2050-97insT
NM_001346900.1:c.2026-98_2026-97insT	NP_001333829.1:n.2026-98_2026-97insT
NM_001346941.1:c.1384-98_1384-97insT	NP_001333870.1:n.1384-98_1384-97insT
NM_005228.4:c.2185-98_2185-97insT	NP_005219.2:n.2185-98_2185-97insT
NM_005228.5:c.2185-98_2185-97insT MANE Select	NP_005219.2:n.2185-98_2185-97insT
NM_001346897.2:c.2050-98_2050-97insT	NP_001333826.1:n.2050-98_2050-97insT
NM_001346898.2:c.2185-98_2185-97insT	NP_001333827.1:n.2185-98_2185-97insT
NM_001346900.2:c.2026-98_2026-97insT	NP_001333829.1:n.2026-98_2026-97insT
NM_001346941.2:c.1384-98_1384-97insT	NP_001333870.1:n.1384-98_1384-97insT
NM_001346899.2:c.2050-98_2050-97insT	NP_001333828.1:n.2050-98_2050-97insT