Canonical Allele Identifier: CA158932361

Gene: EGFR

Linked Data

• dbSNP Id: rs938121064
• gnomAD v3: 7-55174627-G-C
• gnomAD v4: 7-55174627-G-C
• MyVariant Identifiers: chr7:g.55242320G>C (hg19) ; chr7:g.55174627G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174627G>C , CM000669.2:g.55174627G>C	GRCh38
NC_000007.13:g.55242320G>C , CM000669.1:g.55242320G>C	GRCh37
NC_000007.12:g.55209814G>C	NCBI36
NG_007726.3:g.160596G>C , LRG_304:g.160596G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2026-95G>C	ENSP00000413354.2:n.2026-95G>C
ENST00000700145.1:c.534-95G>C
ENST00000275493.7:c.2185-95G>C MANE Select	ENSP00000275493.2:n.2185-95G>C
ENST00000275493.6:c.2185-95G>C	ENSP00000275493.2:n.2185-95G>C
ENST00000442591.5:c.*28+1699G>C	ENSP00000410031.1:n.*28+1699G>C
ENST00000454757.6:c.2050-95G>C	ENSP00000395243.3:n.2050-95G>C
ENST00000455089.5:c.2050-95G>C	ENSP00000415559.1:n.2050-95G>C
NM_005228.3:c.2185-95G>C , LRG_304t1:c.2185-95G>C	NP_005219.2:n.2185-95G>C
NM_001346897.1:c.2050-95G>C	NP_001333826.1:n.2050-95G>C
NM_001346898.1:c.2185-95G>C	NP_001333827.1:n.2185-95G>C
NM_001346899.1:c.2050-95G>C	NP_001333828.1:n.2050-95G>C
NM_001346900.1:c.2026-95G>C	NP_001333829.1:n.2026-95G>C
NM_001346941.1:c.1384-95G>C	NP_001333870.1:n.1384-95G>C
NM_005228.4:c.2185-95G>C	NP_005219.2:n.2185-95G>C
NM_005228.5:c.2185-95G>C MANE Select	NP_005219.2:n.2185-95G>C
NM_001346897.2:c.2050-95G>C	NP_001333826.1:n.2050-95G>C
NM_001346898.2:c.2185-95G>C	NP_001333827.1:n.2185-95G>C
NM_001346900.2:c.2026-95G>C	NP_001333829.1:n.2026-95G>C
NM_001346941.2:c.1384-95G>C	NP_001333870.1:n.1384-95G>C
NM_001346899.2:c.2050-95G>C	NP_001333828.1:n.2050-95G>C