Canonical Allele Identifier: CA135875

Gene: EGFR EGFR-AS1

Linked Data

• ClinVar Variation Id: 45264
• ClinVar RCV Id: RCV000038420
• dbSNP Id: rs397517117
• MyVariant Identifiers: chr7:g.55249031C>T (hg19) ; chr7:g.55181338C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181338C>T , CM000669.2:g.55181338C>T	GRCh38
NC_000007.13:g.55249031C>T , CM000669.1:g.55249031C>T	GRCh37
NC_000007.12:g.55216525C>T	NCBI36
NG_007726.3:g.167307C>T , LRG_304:g.167307C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2170C>T (EGFR)	ENSP00000413354.2:p.Leu724=
ENST00000700145.1:c.678C>T (EGFR)
ENST00000275493.7:c.2329C>T (EGFR) MANE Select	ENSP00000275493.2:p.Leu777=
ENST00000275493.6:c.2329C>T (EGFR)	ENSP00000275493.2:p.Leu777=
ENST00000442591.5:c.*28+8410C>T (EGFR)	ENSP00000410031.1:n.*28+8410C>T
ENST00000454757.6:c.2194C>T (EGFR)	ENSP00000395243.3:p.Leu732=
ENST00000455089.5:c.2194C>T (EGFR)	ENSP00000415559.1:p.Leu732=
NM_005228.3:c.2329C>T , LRG_304t1:c.2329C>T (EGFR)	NP_005219.2:p.Leu777=
NR_047551.1:n.1233G>A (EGFR-AS1)
NM_001346897.1:c.2194C>T (EGFR)	NP_001333826.1:p.Leu732=
NM_001346898.1:c.2329C>T (EGFR)	NP_001333827.1:p.Leu777=
NM_001346899.1:c.2194C>T (EGFR)	NP_001333828.1:p.Leu732=
NM_001346900.1:c.2170C>T (EGFR)	NP_001333829.1:p.Leu724=
NM_001346941.1:c.1528C>T (EGFR)	NP_001333870.1:p.Leu510=
NM_005228.4:c.2329C>T (EGFR)	NP_005219.2:p.Leu777=
NM_005228.5:c.2329C>T (EGFR) MANE Select	NP_005219.2:p.Leu777=
NM_001346897.2:c.2194C>T (EGFR)	NP_001333826.1:p.Leu732=
NM_001346898.2:c.2329C>T (EGFR)	NP_001333827.1:p.Leu777=
NM_001346900.2:c.2170C>T (EGFR)	NP_001333829.1:p.Leu724=
NM_001346941.2:c.1528C>T (EGFR)	NP_001333870.1:p.Leu510=
NM_001346899.2:c.2194C>T (EGFR)	NP_001333828.1:p.Leu732=