Canonical Allele Identifier: CA399314119

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884160C>T (hg19) ; chr17:g.39727907C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727907C>T , CM000679.2:g.39727907C>T	GRCh38
NC_000017.10:g.37884160C>T , CM000679.1:g.37884160C>T	GRCh37
NC_000017.9:g.35137686C>T	NCBI36
NG_007503.1:g.44768C>T , LRG_724:g.44768C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3631C>T MANE Select	ENSP00000269571.4:p.Pro1211Ser
ENST00000269571.9:c.3631C>T	ENSP00000269571.4:p.Pro1211Ser
ENST00000406381.6:c.3541C>T	ENSP00000385185.2:p.Pro1181Ser
ENST00000445658.6:c.2803C>T	ENSP00000404047.2:p.Pro935Ser
ENST00000541774.5:c.3586C>T	ENSP00000446466.1:p.Pro1196Ser
ENST00000578373.5:c.*3421C>T	ENSP00000463427.1:n.*3421C>T
ENST00000584450.5:c.*210C>T	ENSP00000463714.1:n.*210C>T
ENST00000584601.5:c.3541C>T	ENSP00000462438.1:p.Pro1181Ser
NM_001005862.2:c.3541C>T , LRG_724t1:c.3541C>T	NP_001005862.1:p.Pro1181Ser
NM_001289936.1:c.3586C>T , LRG_724t4:c.3586C>T	NP_001276865.1:p.Pro1196Ser
NM_001289937.1:c.*210C>T	NP_001276866.1:n.*210C>T
NM_004448.3:c.3631C>T , LRG_724t2:c.3631C>T	NP_004439.2:p.Pro1211Ser
NR_110535.1:n.3955C>T
XM_024450641.1:c.3769C>T	XP_024306409.1:p.Pro1257Ser
XM_024450642.1:c.3724C>T	XP_024306410.1:p.Pro1242Ser
XM_024450643.1:c.3679C>T	XP_024306411.1:p.Pro1227Ser
NM_001005862.3:c.3541C>T	NP_001005862.1:p.Pro1181Ser
NM_001289936.2:c.3586C>T	NP_001276865.1:p.Pro1196Ser
NM_001289937.2:c.*210C>T	NP_001276866.1:n.*210C>T
NM_001382782.1:c.3541C>T	NP_001369711.1:p.Pro1181Ser
NM_001382783.1:c.3541C>T	NP_001369712.1:p.Pro1181Ser
NM_001382784.1:c.3748C>T	NP_001369713.1:p.Pro1250Ser
NM_001382785.1:c.3733C>T	NP_001369714.1:p.Pro1245Ser
NM_001382786.1:c.3712C>T	NP_001369715.1:p.Pro1238Ser
NM_001382787.1:c.3706C>T	NP_001369716.1:p.Pro1236Ser
NM_001382788.1:c.3661C>T	NP_001369717.1:p.Pro1221Ser
NM_001382789.1:c.3652C>T	NP_001369718.1:p.Pro1218Ser
NM_001382790.1:c.3628C>T	NP_001369719.1:p.Pro1210Ser
NM_001382791.1:c.3622C>T	NP_001369720.1:p.Pro1208Ser
NM_001382792.1:c.3595C>T	NP_001369721.1:p.Pro1199Ser
NM_001382793.1:c.3589C>T	NP_001369722.1:p.Pro1197Ser
NM_001382794.1:c.3589C>T	NP_001369723.1:p.Pro1197Ser
NM_001382795.1:c.3583C>T	NP_001369724.1:p.Pro1195Ser
NM_001382796.1:c.3544C>T	NP_001369725.1:p.Pro1182Ser
NM_001382797.1:c.3532C>T	NP_001369726.1:p.Pro1178Ser
NM_001382798.1:c.3475C>T	NP_001369727.1:p.Pro1159Ser
NM_001382799.1:c.3451C>T	NP_001369728.1:p.Pro1151Ser
NM_001382800.1:c.3445C>T	NP_001369729.1:p.Pro1149Ser
NM_001382801.1:c.3427C>T	NP_001369730.1:p.Pro1143Ser
NM_001382802.1:c.3373C>T	NP_001369731.1:p.Pro1125Ser
NM_001382803.1:c.*210C>T	NP_001369732.1:n.*210C>T
NM_001382804.1:c.2803C>T	NP_001369733.1:p.Pro935Ser
NM_001382805.1:c.2680C>T	NP_001369734.1:p.Pro894Ser
NM_001382806.1:c.2593C>T	NP_001369735.1:p.Pro865Ser
NM_004448.4:c.3631C>T MANE Select	NP_004439.2:p.Pro1211Ser
NR_110535.2:n.3869C>T