Canonical Allele Identifier: CA399314122
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3631C>A MANE Select ENSP00000269571.4:p.Pro1211Thr
ENST00000269571.9:c.3631C>A ENSP00000269571.4:p.Pro1211Thr
ENST00000406381.6:c.3541C>A ENSP00000385185.2:p.Pro1181Thr
ENST00000445658.6:c.2803C>A ENSP00000404047.2:p.Pro935Thr
ENST00000541774.5:c.3586C>A ENSP00000446466.1:p.Pro1196Thr
ENST00000578373.5:c.*3421C>A ENSP00000463427.1:n.*3421C>A
ENST00000584450.5:c.*210C>A ENSP00000463714.1:n.*210C>A
ENST00000584601.5:c.3541C>A ENSP00000462438.1:p.Pro1181Thr
NM_001005862.2:c.3541C>A , LRG_724t1:c.3541C>A NP_001005862.1:p.Pro1181Thr
NM_001289936.1:c.3586C>A , LRG_724t4:c.3586C>A NP_001276865.1:p.Pro1196Thr
NM_001289937.1:c.*210C>A NP_001276866.1:n.*210C>A
NM_004448.3:c.3631C>A , LRG_724t2:c.3631C>A NP_004439.2:p.Pro1211Thr
NR_110535.1:n.3955C>A
XM_024450641.1:c.3769C>A XP_024306409.1:p.Pro1257Thr
XM_024450642.1:c.3724C>A XP_024306410.1:p.Pro1242Thr
XM_024450643.1:c.3679C>A XP_024306411.1:p.Pro1227Thr
NM_001005862.3:c.3541C>A NP_001005862.1:p.Pro1181Thr
NM_001289936.2:c.3586C>A NP_001276865.1:p.Pro1196Thr
NM_001289937.2:c.*210C>A NP_001276866.1:n.*210C>A
NM_001382782.1:c.3541C>A NP_001369711.1:p.Pro1181Thr
NM_001382783.1:c.3541C>A NP_001369712.1:p.Pro1181Thr
NM_001382784.1:c.3748C>A NP_001369713.1:p.Pro1250Thr
NM_001382785.1:c.3733C>A NP_001369714.1:p.Pro1245Thr
NM_001382786.1:c.3712C>A NP_001369715.1:p.Pro1238Thr
NM_001382787.1:c.3706C>A NP_001369716.1:p.Pro1236Thr
NM_001382788.1:c.3661C>A NP_001369717.1:p.Pro1221Thr
NM_001382789.1:c.3652C>A NP_001369718.1:p.Pro1218Thr
NM_001382790.1:c.3628C>A NP_001369719.1:p.Pro1210Thr
NM_001382791.1:c.3622C>A NP_001369720.1:p.Pro1208Thr
NM_001382792.1:c.3595C>A NP_001369721.1:p.Pro1199Thr
NM_001382793.1:c.3589C>A NP_001369722.1:p.Pro1197Thr
NM_001382794.1:c.3589C>A NP_001369723.1:p.Pro1197Thr
NM_001382795.1:c.3583C>A NP_001369724.1:p.Pro1195Thr
NM_001382796.1:c.3544C>A NP_001369725.1:p.Pro1182Thr
NM_001382797.1:c.3532C>A NP_001369726.1:p.Pro1178Thr
NM_001382798.1:c.3475C>A NP_001369727.1:p.Pro1159Thr
NM_001382799.1:c.3451C>A NP_001369728.1:p.Pro1151Thr
NM_001382800.1:c.3445C>A NP_001369729.1:p.Pro1149Thr
NM_001382801.1:c.3427C>A NP_001369730.1:p.Pro1143Thr
NM_001382802.1:c.3373C>A NP_001369731.1:p.Pro1125Thr
NM_001382803.1:c.*210C>A NP_001369732.1:n.*210C>A
NM_001382804.1:c.2803C>A NP_001369733.1:p.Pro935Thr
NM_001382805.1:c.2680C>A NP_001369734.1:p.Pro894Thr
NM_001382806.1:c.2593C>A NP_001369735.1:p.Pro865Thr
NM_004448.4:c.3631C>A MANE Select NP_004439.2:p.Pro1211Thr
NR_110535.2:n.3869C>A