Canonical Allele Identifier: CA2682854820

Gene: EGFR

Linked Data

• gnomAD v4: 7-55174604-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174604G>T , CM000669.2:g.55174604G>T	GRCh38
NC_000007.13:g.55242297G>T , CM000669.1:g.55242297G>T	GRCh37
NC_000007.12:g.55209791G>T	NCBI36
NG_007726.3:g.160573G>T , LRG_304:g.160573G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2026-118G>T	ENSP00000413354.2:n.2026-118G>T
ENST00000700145.1:c.534-118G>T
ENST00000275493.7:c.2185-118G>T MANE Select	ENSP00000275493.2:n.2185-118G>T
ENST00000275493.6:c.2185-118G>T	ENSP00000275493.2:n.2185-118G>T
ENST00000442591.5:c.*28+1676G>T	ENSP00000410031.1:n.*28+1676G>T
ENST00000454757.6:c.2050-118G>T	ENSP00000395243.3:n.2050-118G>T
ENST00000455089.5:c.2050-118G>T	ENSP00000415559.1:n.2050-118G>T
NM_005228.3:c.2185-118G>T , LRG_304t1:c.2185-118G>T	NP_005219.2:n.2185-118G>T
NM_001346897.1:c.2050-118G>T	NP_001333826.1:n.2050-118G>T
NM_001346898.1:c.2185-118G>T	NP_001333827.1:n.2185-118G>T
NM_001346899.1:c.2050-118G>T	NP_001333828.1:n.2050-118G>T
NM_001346900.1:c.2026-118G>T	NP_001333829.1:n.2026-118G>T
NM_001346941.1:c.1384-118G>T	NP_001333870.1:n.1384-118G>T
NM_005228.4:c.2185-118G>T	NP_005219.2:n.2185-118G>T
NM_005228.5:c.2185-118G>T MANE Select	NP_005219.2:n.2185-118G>T
NM_001346897.2:c.2050-118G>T	NP_001333826.1:n.2050-118G>T
NM_001346898.2:c.2185-118G>T	NP_001333827.1:n.2185-118G>T
NM_001346900.2:c.2026-118G>T	NP_001333829.1:n.2026-118G>T
NM_001346941.2:c.1384-118G>T	NP_001333870.1:n.1384-118G>T
NM_001346899.2:c.2050-118G>T	NP_001333828.1:n.2050-118G>T