Canonical Allele Identifier: CA367580120
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs397517126
MyVariant Identifiers: chr7:g.55259439T>A (hg19) chr7:g.55191746T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55191746T>A , CM000669.2:g.55191746T>A GRCh38
NC_000007.13:g.55259439T>A , CM000669.1:g.55259439T>A GRCh37
NC_000007.12:g.55226933T>A NCBI36
NG_007726.3:g.177715T>A , LRG_304:g.177715T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2338T>A ENSP00000413354.2:p.Leu780Met
ENST00000700145.1:c.846T>A
ENST00000275493.7:c.2497T>A MANE Select ENSP00000275493.2:p.Leu833Met
ENST00000275493.6:c.2497T>A ENSP00000275493.2:p.Leu833Met
ENST00000442591.5:c.*28+18818T>A ENSP00000410031.1:n.*28+18818T>A
ENST00000454757.6:c.2362T>A ENSP00000395243.3:p.Leu788Met
ENST00000455089.5:c.2362T>A ENSP00000415559.1:p.Leu788Met
NM_005228.3:c.2497T>A , LRG_304t1:c.2497T>A NP_005219.2:p.Leu833Met
NM_001346897.1:c.2362T>A NP_001333826.1:p.Leu788Met
NM_001346898.1:c.2497T>A NP_001333827.1:p.Leu833Met
NM_001346899.1:c.2362T>A NP_001333828.1:p.Leu788Met
NM_001346900.1:c.2338T>A NP_001333829.1:p.Leu780Met
NM_001346941.1:c.1696T>A NP_001333870.1:p.Leu566Met
NM_005228.4:c.2497T>A NP_005219.2:p.Leu833Met
NM_005228.5:c.2497T>A MANE Select NP_005219.2:p.Leu833Met
NM_001346897.2:c.2362T>A NP_001333826.1:p.Leu788Met
NM_001346898.2:c.2497T>A NP_001333827.1:p.Leu833Met
NM_001346900.2:c.2338T>A NP_001333829.1:p.Leu780Met
NM_001346941.2:c.1696T>A NP_001333870.1:p.Leu566Met
NM_001346899.2:c.2362T>A NP_001333828.1:p.Leu788Met
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