Canonical Allele Identifier: CA454965660
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs2128964655
MyVariant Identifiers: chr7:g.55259528G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55191835G>T , CM000669.2:g.55191835G>T GRCh38
NC_000007.13:g.55259528G>T , CM000669.1:g.55259528G>T GRCh37
NC_000007.12:g.55227022G>T NCBI36
NG_007726.3:g.177804G>T , LRG_304:g.177804G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2427G>T ENSP00000413354.2:p.Leu809=
ENST00000700145.1:c.899+36G>T
ENST00000275493.7:c.2586G>T MANE Select ENSP00000275493.2:p.Leu862=
ENST00000275493.6:c.2586G>T ENSP00000275493.2:p.Leu862=
ENST00000442591.5:c.*28+18907G>T ENSP00000410031.1:n.*28+18907G>T
ENST00000454757.6:c.2451G>T ENSP00000395243.3:p.Leu817=
ENST00000455089.5:c.2451G>T ENSP00000415559.1:p.Leu817=
NM_005228.3:c.2586G>T , LRG_304t1:c.2586G>T NP_005219.2:p.Leu862=
NM_001346897.1:c.2451G>T NP_001333826.1:p.Leu817=
NM_001346898.1:c.2586G>T NP_001333827.1:p.Leu862=
NM_001346899.1:c.2451G>T NP_001333828.1:p.Leu817=
NM_001346900.1:c.2427G>T NP_001333829.1:p.Leu809=
NM_001346941.1:c.1785G>T NP_001333870.1:p.Leu595=
NM_005228.4:c.2586G>T NP_005219.2:p.Leu862=
NM_005228.5:c.2586G>T MANE Select NP_005219.2:p.Leu862=
NM_001346897.2:c.2451G>T NP_001333826.1:p.Leu817=
NM_001346898.2:c.2586G>T NP_001333827.1:p.Leu862=
NM_001346900.2:c.2427G>T NP_001333829.1:p.Leu809=
NM_001346941.2:c.1785G>T NP_001333870.1:p.Leu595=
NM_001346899.2:c.2451G>T NP_001333828.1:p.Leu817=