Canonical Allele Identifier: CA399314160

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884167T>G (hg19) ; chr17:g.39727914T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727914T>G , CM000679.2:g.39727914T>G	GRCh38
NC_000017.10:g.37884167T>G , CM000679.1:g.37884167T>G	GRCh37
NC_000017.9:g.35137693T>G	NCBI36
NG_007503.1:g.44775T>G , LRG_724:g.44775T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3638T>G MANE Select	ENSP00000269571.4:p.Phe1213Cys
ENST00000269571.9:c.3638T>G	ENSP00000269571.4:p.Phe1213Cys
ENST00000406381.6:c.3548T>G	ENSP00000385185.2:p.Phe1183Cys
ENST00000445658.6:c.2810T>G	ENSP00000404047.2:p.Phe937Cys
ENST00000541774.5:c.3593T>G	ENSP00000446466.1:p.Phe1198Cys
ENST00000578373.5:c.*3428T>G	ENSP00000463427.1:n.*3428T>G
ENST00000584450.5:c.*217T>G	ENSP00000463714.1:n.*217T>G
ENST00000584601.5:c.3548T>G	ENSP00000462438.1:p.Phe1183Cys
NM_001005862.2:c.3548T>G , LRG_724t1:c.3548T>G	NP_001005862.1:p.Phe1183Cys
NM_001289936.1:c.3593T>G , LRG_724t4:c.3593T>G	NP_001276865.1:p.Phe1198Cys
NM_001289937.1:c.*217T>G	NP_001276866.1:n.*217T>G
NM_004448.3:c.3638T>G , LRG_724t2:c.3638T>G	NP_004439.2:p.Phe1213Cys
NR_110535.1:n.3962T>G
XM_024450641.1:c.3776T>G	XP_024306409.1:p.Phe1259Cys
XM_024450642.1:c.3731T>G	XP_024306410.1:p.Phe1244Cys
XM_024450643.1:c.3686T>G	XP_024306411.1:p.Phe1229Cys
NM_001005862.3:c.3548T>G	NP_001005862.1:p.Phe1183Cys
NM_001289936.2:c.3593T>G	NP_001276865.1:p.Phe1198Cys
NM_001289937.2:c.*217T>G	NP_001276866.1:n.*217T>G
NM_001382782.1:c.3548T>G	NP_001369711.1:p.Phe1183Cys
NM_001382783.1:c.3548T>G	NP_001369712.1:p.Phe1183Cys
NM_001382784.1:c.3755T>G	NP_001369713.1:p.Phe1252Cys
NM_001382785.1:c.3740T>G	NP_001369714.1:p.Phe1247Cys
NM_001382786.1:c.3719T>G	NP_001369715.1:p.Phe1240Cys
NM_001382787.1:c.3713T>G	NP_001369716.1:p.Phe1238Cys
NM_001382788.1:c.3668T>G	NP_001369717.1:p.Phe1223Cys
NM_001382789.1:c.3659T>G	NP_001369718.1:p.Phe1220Cys
NM_001382790.1:c.3635T>G	NP_001369719.1:p.Phe1212Cys
NM_001382791.1:c.3629T>G	NP_001369720.1:p.Phe1210Cys
NM_001382792.1:c.3602T>G	NP_001369721.1:p.Phe1201Cys
NM_001382793.1:c.3596T>G	NP_001369722.1:p.Phe1199Cys
NM_001382794.1:c.3596T>G	NP_001369723.1:p.Phe1199Cys
NM_001382795.1:c.3590T>G	NP_001369724.1:p.Phe1197Cys
NM_001382796.1:c.3551T>G	NP_001369725.1:p.Phe1184Cys
NM_001382797.1:c.3539T>G	NP_001369726.1:p.Phe1180Cys
NM_001382798.1:c.3482T>G	NP_001369727.1:p.Phe1161Cys
NM_001382799.1:c.3458T>G	NP_001369728.1:p.Phe1153Cys
NM_001382800.1:c.3452T>G	NP_001369729.1:p.Phe1151Cys
NM_001382801.1:c.3434T>G	NP_001369730.1:p.Phe1145Cys
NM_001382802.1:c.3380T>G	NP_001369731.1:p.Phe1127Cys
NM_001382803.1:c.*217T>G	NP_001369732.1:n.*217T>G
NM_001382804.1:c.2810T>G	NP_001369733.1:p.Phe937Cys
NM_001382805.1:c.2687T>G	NP_001369734.1:p.Phe896Cys
NM_001382806.1:c.2600T>G	NP_001369735.1:p.Phe867Cys
NM_004448.4:c.3638T>G MANE Select	NP_004439.2:p.Phe1213Cys
NR_110535.2:n.3876T>G