Canonical Allele Identifier: CA158930100
Gene: EGFR HGNC NCBI
EGFR-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs749353415
gnomAD v3: 7-55183821-C-A
gnomAD v4: 7-55183821-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55183821C>A , CM000669.2:g.55183821C>A GRCh38
NC_000007.13:g.55251514C>A , CM000669.1:g.55251514C>A GRCh37
NC_000007.12:g.55219008C>A NCBI36
NG_007726.3:g.169790C>A , LRG_304:g.169790C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2310+2343C>A (EGFR) ENSP00000413354.2:n.2310+2343C>A
ENST00000700145.1:c.818+2343C>A (EGFR)
ENST00000275493.7:c.2469+2343C>A (EGFR) MANE Select ENSP00000275493.2:n.2469+2343C>A
ENST00000275493.6:c.2469+2343C>A (EGFR) ENSP00000275493.2:n.2469+2343C>A
ENST00000442591.5:c.*28+10893C>A (EGFR) ENSP00000410031.1:n.*28+10893C>A
ENST00000454757.6:c.2334+2343C>A (EGFR) ENSP00000395243.3:n.2334+2343C>A
ENST00000455089.5:c.2334+2343C>A (EGFR) ENSP00000415559.1:n.2334+2343C>A
NM_005228.3:c.2469+2343C>A , LRG_304t1:c.2469+2343C>A (EGFR) NP_005219.2:n.2469+2343C>A
NR_047551.1:n.94-1344G>T (EGFR-AS1)
NM_001346897.1:c.2334+2343C>A (EGFR) NP_001333826.1:n.2334+2343C>A
NM_001346898.1:c.2469+2343C>A (EGFR) NP_001333827.1:n.2469+2343C>A
NM_001346899.1:c.2334+2343C>A (EGFR) NP_001333828.1:n.2334+2343C>A
NM_001346900.1:c.2310+2343C>A (EGFR) NP_001333829.1:n.2310+2343C>A
NM_001346941.1:c.1668+2343C>A (EGFR) NP_001333870.1:n.1668+2343C>A
NM_005228.4:c.2469+2343C>A (EGFR) NP_005219.2:n.2469+2343C>A
NM_005228.5:c.2469+2343C>A (EGFR) MANE Select NP_005219.2:n.2469+2343C>A
NM_001346897.2:c.2334+2343C>A (EGFR) NP_001333826.1:n.2334+2343C>A
NM_001346898.2:c.2469+2343C>A (EGFR) NP_001333827.1:n.2469+2343C>A
NM_001346900.2:c.2310+2343C>A (EGFR) NP_001333829.1:n.2310+2343C>A
NM_001346941.2:c.1668+2343C>A (EGFR) NP_001333870.1:n.1668+2343C>A
NM_001346899.2:c.2334+2343C>A (EGFR) NP_001333828.1:n.2334+2343C>A