Canonical Allele Identifier: CA454968527

Gene: EGFR

Linked Data

• MyVariant Identifiers: chr7:g.55268913A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55201220A>C , CM000669.2:g.55201220A>C	GRCh38
NC_000007.13:g.55268913A>C , CM000669.1:g.55268913A>C	GRCh37
NC_000007.12:g.55236407A>C	NCBI36
NG_007726.3:g.187189A>C , LRG_304:g.187189A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2820A>C	ENSP00000413354.2:p.Thr940=
ENST00000700145.1:c.900-4127A>C
ENST00000700146.1:n.723A>C
ENST00000700147.1:n.648A>C
ENST00000275493.7:c.2979A>C MANE Select	ENSP00000275493.2:p.Thr993=
ENST00000275493.6:c.2979A>C	ENSP00000275493.2:p.Thr993=
ENST00000442591.5:c.*28+28292A>C	ENSP00000410031.1:n.*28+28292A>C
ENST00000454757.6:c.2844A>C	ENSP00000395243.3:p.Thr948=
ENST00000455089.5:c.2844A>C	ENSP00000415559.1:p.Thr948=
NM_005228.3:c.2979A>C , LRG_304t1:c.2979A>C	NP_005219.2:p.Thr993=
NM_001346897.1:c.2844A>C	NP_001333826.1:p.Thr948=
NM_001346898.1:c.2979A>C	NP_001333827.1:p.Thr993=
NM_001346899.1:c.2844A>C	NP_001333828.1:p.Thr948=
NM_001346900.1:c.2820A>C	NP_001333829.1:p.Thr940=
NM_001346941.1:c.2178A>C	NP_001333870.1:p.Thr726=
NM_005228.4:c.2979A>C	NP_005219.2:p.Thr993=
NM_005228.5:c.2979A>C MANE Select	NP_005219.2:p.Thr993=
NM_001346897.2:c.2844A>C	NP_001333826.1:p.Thr948=
NM_001346898.2:c.2979A>C	NP_001333827.1:p.Thr993=
NM_001346900.2:c.2820A>C	NP_001333829.1:p.Thr940=
NM_001346941.2:c.2178A>C	NP_001333870.1:p.Thr726=
NM_001346899.2:c.2844A>C	NP_001333828.1:p.Thr948=