Canonical Allele Identifier: CA2714924094

Gene: EGFR EGFR-AS1

Linked Data

• dbSNP Id: rs2128957933

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181172del , CM000669.2:g.55181172del	GRCh38
NC_000007.13:g.55248865del , CM000669.1:g.55248865del	GRCh37
NC_000007.12:g.55216359del	NCBI36
NG_007726.3:g.167141del , LRG_304:g.167141del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2125-121del (EGFR)	ENSP00000413354.2:n.2125-121del
ENST00000700145.1:c.633-121del (EGFR)
ENST00000275493.7:c.2284-121del (EGFR) MANE Select	ENSP00000275493.2:n.2284-121del
ENST00000275493.6:c.2284-121del (EGFR)	ENSP00000275493.2:n.2284-121del
ENST00000442591.5:c.*28+8244del (EGFR)	ENSP00000410031.1:n.*28+8244del
ENST00000454757.6:c.2149-121del (EGFR)	ENSP00000395243.3:n.2149-121del
ENST00000455089.5:c.2149-121del (EGFR)	ENSP00000415559.1:n.2149-121del
NM_005228.3:c.2284-121del , LRG_304t1:c.2284-121del (EGFR)	NP_005219.2:n.2284-121del
NR_047551.1:n.1400del (EGFR-AS1)
NM_001346897.1:c.2149-121del (EGFR)	NP_001333826.1:n.2149-121del
NM_001346898.1:c.2284-121del (EGFR)	NP_001333827.1:n.2284-121del
NM_001346899.1:c.2149-121del (EGFR)	NP_001333828.1:n.2149-121del
NM_001346900.1:c.2125-121del (EGFR)	NP_001333829.1:n.2125-121del
NM_001346941.1:c.1483-121del (EGFR)	NP_001333870.1:n.1483-121del
NM_005228.4:c.2284-121del (EGFR)	NP_005219.2:n.2284-121del
NM_005228.5:c.2284-121del (EGFR) MANE Select	NP_005219.2:n.2284-121del
NM_001346897.2:c.2149-121del (EGFR)	NP_001333826.1:n.2149-121del
NM_001346898.2:c.2284-121del (EGFR)	NP_001333827.1:n.2284-121del
NM_001346900.2:c.2125-121del (EGFR)	NP_001333829.1:n.2125-121del
NM_001346941.2:c.1483-121del (EGFR)	NP_001333870.1:n.1483-121del
NM_001346899.2:c.2149-121del (EGFR)	NP_001333828.1:n.2149-121del