Canonical Allele Identifier: CA645561593
Gene: EGFR HGNC NCBI
EGFR-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2128958391

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55181320_55181321insGCGTCGAAA , CM000669.2:g.55181320_55181321insGCGTCGAAA GRCh38
NC_000007.13:g.55249013_55249014insGCGTCGAAA , CM000669.1:g.55249013_55249014insGCGTCGAAA GRCh37
NC_000007.12:g.55216507_55216508insGCGTCGAAA NCBI36
NG_007726.3:g.167289_167290insGCGTCGAAA , LRG_304:g.167289_167290insGCGTCGAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000450046.2:c.2152_2153insGCGTCGAAA (EGFR) ENSP00000413354.2:p.Asp717_Asn718insSerValGlu
ENST00000700145.1:c.660_661insGCGTCGAAA (EGFR)
ENST00000275493.7:c.2311_2312insGCGTCGAAA (EGFR) MANE Select ENSP00000275493.2:p.Asp770_Asn771insSerValGlu
ENST00000275493.6:c.2311_2312insGCGTCGAAA (EGFR) ENSP00000275493.2:p.Asp770_Asn771insSerValGlu
ENST00000442591.5:c.*28+8392_*28+8393insGCGTCGAAA (EGFR) ENSP00000410031.1:n.*28+8392_*28+8393insGCGTCGAAA
ENST00000454757.6:c.2176_2177insGCGTCGAAA (EGFR) ENSP00000395243.3:p.Asp725_Asn726insSerValGlu
ENST00000455089.5:c.2176_2177insGCGTCGAAA (EGFR) ENSP00000415559.1:p.Asp725_Asn726insSerValGlu
NM_005228.3:c.2311_2312insGCGTCGAAA , LRG_304t1:c.2311_2312insGCGTCGAAA (EGFR) NP_005219.2:p.Asp770_Asn771insSerValGlu
NR_047551.1:n.1251_1252insTTCGACGCT (EGFR-AS1)
NM_001346897.1:c.2176_2177insGCGTCGAAA (EGFR) NP_001333826.1:p.Asp725_Asn726insSerValGlu
NM_001346898.1:c.2311_2312insGCGTCGAAA (EGFR) NP_001333827.1:p.Asp770_Asn771insSerValGlu
NM_001346899.1:c.2176_2177insGCGTCGAAA (EGFR) NP_001333828.1:p.Asp725_Asn726insSerValGlu
NM_001346900.1:c.2152_2153insGCGTCGAAA (EGFR) NP_001333829.1:p.Asp717_Asn718insSerValGlu
NM_001346941.1:c.1510_1511insGCGTCGAAA (EGFR) NP_001333870.1:p.Asp503_Asn504insSerValGlu
NM_005228.4:c.2311_2312insGCGTCGAAA (EGFR) NP_005219.2:p.Asp770_Asn771insSerValGlu
NM_005228.5:c.2311_2312insGCGTCGAAA (EGFR) MANE Select NP_005219.2:p.Asp770_Asn771insSerValGlu
NM_001346897.2:c.2176_2177insGCGTCGAAA (EGFR) NP_001333826.1:p.Asp725_Asn726insSerValGlu
NM_001346898.2:c.2311_2312insGCGTCGAAA (EGFR) NP_001333827.1:p.Asp770_Asn771insSerValGlu
NM_001346900.2:c.2152_2153insGCGTCGAAA (EGFR) NP_001333829.1:p.Asp717_Asn718insSerValGlu
NM_001346941.2:c.1510_1511insGCGTCGAAA (EGFR) NP_001333870.1:p.Asp503_Asn504insSerValGlu
NM_001346899.2:c.2176_2177insGCGTCGAAA (EGFR) NP_001333828.1:p.Asp725_Asn726insSerValGlu