Canonical Allele Identifier: CA645561538
Gene: EGFR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174785_55174813delinsCCAAC , CM000669.2:g.55174785_55174813delinsCCAAC GRCh38
NC_000007.13:g.55242478_55242506delinsCCAAC , CM000669.1:g.55242478_55242506delinsCCAAC GRCh37
NC_000007.12:g.55209972_55210000delinsCCAAC NCBI36
NG_007726.3:g.160754_160782delinsCCAAC , LRG_304:g.160754_160782delinsCCAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2089_2117delinsCCAAC ENSP00000413354.2:p.Ala697_Ile706delinsPr...
ENST00000700145.1:c.597_625delinsCCAAC
ENST00000275493.7:c.2248_2276delinsCCAAC MANE Select ENSP00000275493.2:p.Ala750_Ile759delinsPr...
ENST00000275493.6:c.2248_2276delinsCCAAC ENSP00000275493.2:p.Ala750_Ile759delinsPr...
ENST00000442591.5:c.*28+1857_*28+1885delinsCCAAC ENSP00000410031.1:n.*28+1857_*28+1885deli...
ENST00000454757.6:c.2113_2141delinsCCAAC ENSP00000395243.3:p.Ala705_Ile714delinsPr...
ENST00000455089.5:c.2113_2141delinsCCAAC ENSP00000415559.1:p.Ala705_Ile714delinsPr...
NM_005228.3:c.2248_2276delinsCCAAC , LRG_304t1:c.2248_2276delinsCCAAC NP_005219.2:p.Ala750_Ile759delinsProThr
NM_001346897.1:c.2113_2141delinsCCAAC NP_001333826.1:p.Ala705_Ile714delinsProTh...
NM_001346898.1:c.2248_2276delinsCCAAC NP_001333827.1:p.Ala750_Ile759delinsProTh...
NM_001346899.1:c.2113_2141delinsCCAAC NP_001333828.1:p.Ala705_Ile714delinsProTh...
NM_001346900.1:c.2089_2117delinsCCAAC NP_001333829.1:p.Ala697_Ile706delinsProTh...
NM_001346941.1:c.1447_1475delinsCCAAC NP_001333870.1:p.Ala483_Ile492delinsProTh...
NM_005228.4:c.2248_2276delinsCCAAC NP_005219.2:p.Ala750_Ile759delinsProThr
NM_005228.5:c.2248_2276delinsCCAAC MANE Select NP_005219.2:p.Ala750_Ile759delinsProThr
NM_001346897.2:c.2113_2141delinsCCAAC NP_001333826.1:p.Ala705_Ile714delinsProTh...
NM_001346898.2:c.2248_2276delinsCCAAC NP_001333827.1:p.Ala750_Ile759delinsProTh...
NM_001346900.2:c.2089_2117delinsCCAAC NP_001333829.1:p.Ala697_Ile706delinsProTh...
NM_001346941.2:c.1447_1475delinsCCAAC NP_001333870.1:p.Ala483_Ile492delinsProTh...
NM_001346899.2:c.2113_2141delinsCCAAC NP_001333828.1:p.Ala705_Ile714delinsProTh...