Canonical Allele Identifier: CA454965625

Gene: EGFR

Linked Data

• MyVariant Identifiers: chr7:g.55259477G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191784G>T , CM000669.2:g.55191784G>T	GRCh38
NC_000007.13:g.55259477G>T , CM000669.1:g.55259477G>T	GRCh37
NC_000007.12:g.55226971G>T	NCBI36
NG_007726.3:g.177753G>T , LRG_304:g.177753G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2376G>T	ENSP00000413354.2:p.Val792=
ENST00000700145.1:c.884G>T
ENST00000275493.7:c.2535G>T MANE Select	ENSP00000275493.2:p.Val845=
ENST00000275493.6:c.2535G>T	ENSP00000275493.2:p.Val845=
ENST00000442591.5:c.*28+18856G>T	ENSP00000410031.1:n.*28+18856G>T
ENST00000454757.6:c.2400G>T	ENSP00000395243.3:p.Val800=
ENST00000455089.5:c.2400G>T	ENSP00000415559.1:p.Val800=
NM_005228.3:c.2535G>T , LRG_304t1:c.2535G>T	NP_005219.2:p.Val845=
NM_001346897.1:c.2400G>T	NP_001333826.1:p.Val800=
NM_001346898.1:c.2535G>T	NP_001333827.1:p.Val845=
NM_001346899.1:c.2400G>T	NP_001333828.1:p.Val800=
NM_001346900.1:c.2376G>T	NP_001333829.1:p.Val792=
NM_001346941.1:c.1734G>T	NP_001333870.1:p.Val578=
NM_005228.4:c.2535G>T	NP_005219.2:p.Val845=
NM_005228.5:c.2535G>T MANE Select	NP_005219.2:p.Val845=
NM_001346897.2:c.2400G>T	NP_001333826.1:p.Val800=
NM_001346898.2:c.2535G>T	NP_001333827.1:p.Val845=
NM_001346900.2:c.2376G>T	NP_001333829.1:p.Val792=
NM_001346941.2:c.1734G>T	NP_001333870.1:p.Val578=
NM_001346899.2:c.2400G>T	NP_001333828.1:p.Val800=