Canonical Allele Identifier: CA2714923112

Gene: EGFR

Linked Data

• dbSNP Id: rs2128860113

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55027508_55027509insTGGTTTT , CM000669.2:g.55027508_55027509insTGGTTTT	GRCh38
NC_000007.13:g.55095201_55095202insTGGTTTT , CM000669.1:g.55095201_55095202insTGGTTTT	GRCh37
NC_000007.12:g.55062695_55062696insTGGTTTT	NCBI36
NG_007726.3:g.13477_13478insTGGTTTT , LRG_304:g.13477_13478insTGGTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000459688.2:n.235+8143_235+8144insTGGTTTT
ENST00000700144.1:n.278+8143_278+8144insTGGTTTT
ENST00000344576.7:c.88+8143_88+8144insTGGTTTT	ENSP00000345973.2:n.88+8143_88+8144insTGGTTTT
ENST00000275493.7:c.88+8143_88+8144insTGGTTTT MANE Select	ENSP00000275493.2:n.88+8143_88+8144insTGGTTTT
ENST00000275493.6:c.88+8143_88+8144insTGGTTTT	ENSP00000275493.2:n.88+8143_88+8144insTGGTTTT
ENST00000342916.7:c.88+8143_88+8144insTGGTTTT	ENSP00000342376.3:n.88+8143_88+8144insTGGTTTT
ENST00000344576.6:c.88+8143_88+8144insTGGTTTT	ENSP00000345973.2:n.88+8143_88+8144insTGGTTTT
ENST00000420316.6:c.88+8143_88+8144insTGGTTTT	ENSP00000413843.2:n.88+8143_88+8144insTGGTTTT
ENST00000442591.5:c.88+8143_88+8144insTGGTTTT	ENSP00000410031.1:n.88+8143_88+8144insTGGTTTT
ENST00000454757.6:c.88+8143_88+8144insTGGTTTT	ENSP00000395243.3:n.88+8143_88+8144insTGGTTTT
ENST00000455089.5:c.88+8143_88+8144insTGGTTTT	ENSP00000415559.1:n.88+8143_88+8144insTGGTTTT
ENST00000459688.1:n.235+8143_235+8144insTGGTTTT
ENST00000463948.1:n.215+8143_215+8144insTGGTTTT
NM_005228.3:c.88+8143_88+8144insTGGTTTT , LRG_304t1:c.88+8143_88+8144insTGGTTTT	NP_005219.2:n.88+8143_88+8144insTGGTTTT
NM_201282.1:c.88+8143_88+8144insTGGTTTT	NP_958439.1:n.88+8143_88+8144insTGGTTTT
NM_201283.1:c.88+8143_88+8144insTGGTTTT	NP_958440.1:n.88+8143_88+8144insTGGTTTT
NM_201284.1:c.88+8143_88+8144insTGGTTTT	NP_958441.1:n.88+8143_88+8144insTGGTTTT
NM_001346897.1:c.88+8143_88+8144insTGGTTTT	NP_001333826.1:n.88+8143_88+8144insTGGTTTT
NM_001346898.1:c.88+8143_88+8144insTGGTTTT	NP_001333827.1:n.88+8143_88+8144insTGGTTTT
NM_001346899.1:c.88+8143_88+8144insTGGTTTT	NP_001333828.1:n.88+8143_88+8144insTGGTTTT
NM_001346941.1:c.88+8143_88+8144insTGGTTTT	NP_001333870.1:n.88+8143_88+8144insTGGTTTT
NM_005228.4:c.88+8143_88+8144insTGGTTTT	NP_005219.2:n.88+8143_88+8144insTGGTTTT
NM_005228.5:c.88+8143_88+8144insTGGTTTT MANE Select	NP_005219.2:n.88+8143_88+8144insTGGTTTT
NM_001346897.2:c.88+8143_88+8144insTGGTTTT	NP_001333826.1:n.88+8143_88+8144insTGGTTTT
NM_001346898.2:c.88+8143_88+8144insTGGTTTT	NP_001333827.1:n.88+8143_88+8144insTGGTTTT
NM_001346941.2:c.88+8143_88+8144insTGGTTTT	NP_001333870.1:n.88+8143_88+8144insTGGTTTT
NM_201282.2:c.88+8143_88+8144insTGGTTTT	NP_958439.1:n.88+8143_88+8144insTGGTTTT
NM_201284.2:c.88+8143_88+8144insTGGTTTT	NP_958441.1:n.88+8143_88+8144insTGGTTTT
NM_001346899.2:c.88+8143_88+8144insTGGTTTT	NP_001333828.1:n.88+8143_88+8144insTGGTTTT
NM_201283.2:c.88+8143_88+8144insTGGTTTT	NP_958440.1:n.88+8143_88+8144insTGGTTTT