Canonical Allele Identifier: CA455165167

Gene: EGFR EGFR-AS1

Linked Data

• dbSNP Id: rs376452156
• MyVariant Identifiers: chr7:g.55249072G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181379G>C , CM000669.2:g.55181379G>C	GRCh38
NC_000007.13:g.55249072G>C , CM000669.1:g.55249072G>C	GRCh37
NC_000007.12:g.55216566G>C	NCBI36
NG_007726.3:g.167348G>C , LRG_304:g.167348G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2211G>C (EGFR)	ENSP00000413354.2:p.Thr737=
ENST00000700145.1:c.719G>C (EGFR)
ENST00000275493.7:c.2370G>C (EGFR) MANE Select	ENSP00000275493.2:p.Thr790=
ENST00000275493.6:c.2370G>C (EGFR)	ENSP00000275493.2:p.Thr790=
ENST00000442591.5:c.*28+8451G>C (EGFR)	ENSP00000410031.1:n.*28+8451G>C
ENST00000454757.6:c.2235G>C (EGFR)	ENSP00000395243.3:p.Thr745=
ENST00000455089.5:c.2235G>C (EGFR)	ENSP00000415559.1:p.Thr745=
NM_005228.3:c.2370G>C , LRG_304t1:c.2370G>C (EGFR)	NP_005219.2:p.Thr790=
NR_047551.1:n.1192C>G (EGFR-AS1)
NM_001346897.1:c.2235G>C (EGFR)	NP_001333826.1:p.Thr745=
NM_001346898.1:c.2370G>C (EGFR)	NP_001333827.1:p.Thr790=
NM_001346899.1:c.2235G>C (EGFR)	NP_001333828.1:p.Thr745=
NM_001346900.1:c.2211G>C (EGFR)	NP_001333829.1:p.Thr737=
NM_001346941.1:c.1569G>C (EGFR)	NP_001333870.1:p.Thr523=
NM_005228.4:c.2370G>C (EGFR)	NP_005219.2:p.Thr790=
NM_005228.5:c.2370G>C (EGFR) MANE Select	NP_005219.2:p.Thr790=
NM_001346897.2:c.2235G>C (EGFR)	NP_001333826.1:p.Thr745=
NM_001346898.2:c.2370G>C (EGFR)	NP_001333827.1:p.Thr790=
NM_001346900.2:c.2211G>C (EGFR)	NP_001333829.1:p.Thr737=
NM_001346941.2:c.1569G>C (EGFR)	NP_001333870.1:p.Thr523=
NM_001346899.2:c.2235G>C (EGFR)	NP_001333828.1:p.Thr745=