Canonical Allele Identifier: CA399314087

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059869654
• MyVariant Identifiers: chr17:g.37884157C>A (hg19) ; chr17:g.39727904C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727904C>A , CM000679.2:g.39727904C>A	GRCh38
NC_000017.10:g.37884157C>A , CM000679.1:g.37884157C>A	GRCh37
NC_000017.9:g.35137683C>A	NCBI36
NG_007503.1:g.44765C>A , LRG_724:g.44765C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3628C>A MANE Select	ENSP00000269571.4:p.Pro1210Thr
ENST00000269571.9:c.3628C>A	ENSP00000269571.4:p.Pro1210Thr
ENST00000406381.6:c.3538C>A	ENSP00000385185.2:p.Pro1180Thr
ENST00000445658.6:c.2800C>A	ENSP00000404047.2:p.Pro934Thr
ENST00000541774.5:c.3583C>A	ENSP00000446466.1:p.Pro1195Thr
ENST00000578373.5:c.*3418C>A	ENSP00000463427.1:n.*3418C>A
ENST00000584450.5:c.*207C>A	ENSP00000463714.1:n.*207C>A
ENST00000584601.5:c.3538C>A	ENSP00000462438.1:p.Pro1180Thr
NM_001005862.2:c.3538C>A , LRG_724t1:c.3538C>A	NP_001005862.1:p.Pro1180Thr
NM_001289936.1:c.3583C>A , LRG_724t4:c.3583C>A	NP_001276865.1:p.Pro1195Thr
NM_001289937.1:c.*207C>A	NP_001276866.1:n.*207C>A
NM_004448.3:c.3628C>A , LRG_724t2:c.3628C>A	NP_004439.2:p.Pro1210Thr
NR_110535.1:n.3952C>A
XM_024450641.1:c.3766C>A	XP_024306409.1:p.Pro1256Thr
XM_024450642.1:c.3721C>A	XP_024306410.1:p.Pro1241Thr
XM_024450643.1:c.3676C>A	XP_024306411.1:p.Pro1226Thr
NM_001005862.3:c.3538C>A	NP_001005862.1:p.Pro1180Thr
NM_001289936.2:c.3583C>A	NP_001276865.1:p.Pro1195Thr
NM_001289937.2:c.*207C>A	NP_001276866.1:n.*207C>A
NM_001382782.1:c.3538C>A	NP_001369711.1:p.Pro1180Thr
NM_001382783.1:c.3538C>A	NP_001369712.1:p.Pro1180Thr
NM_001382784.1:c.3745C>A	NP_001369713.1:p.Pro1249Thr
NM_001382785.1:c.3730C>A	NP_001369714.1:p.Pro1244Thr
NM_001382786.1:c.3709C>A	NP_001369715.1:p.Pro1237Thr
NM_001382787.1:c.3703C>A	NP_001369716.1:p.Pro1235Thr
NM_001382788.1:c.3658C>A	NP_001369717.1:p.Pro1220Thr
NM_001382789.1:c.3649C>A	NP_001369718.1:p.Pro1217Thr
NM_001382790.1:c.3625C>A	NP_001369719.1:p.Pro1209Thr
NM_001382791.1:c.3619C>A	NP_001369720.1:p.Pro1207Thr
NM_001382792.1:c.3592C>A	NP_001369721.1:p.Pro1198Thr
NM_001382793.1:c.3586C>A	NP_001369722.1:p.Pro1196Thr
NM_001382794.1:c.3586C>A	NP_001369723.1:p.Pro1196Thr
NM_001382795.1:c.3580C>A	NP_001369724.1:p.Pro1194Thr
NM_001382796.1:c.3541C>A	NP_001369725.1:p.Pro1181Thr
NM_001382797.1:c.3529C>A	NP_001369726.1:p.Pro1177Thr
NM_001382798.1:c.3472C>A	NP_001369727.1:p.Pro1158Thr
NM_001382799.1:c.3448C>A	NP_001369728.1:p.Pro1150Thr
NM_001382800.1:c.3442C>A	NP_001369729.1:p.Pro1148Thr
NM_001382801.1:c.3424C>A	NP_001369730.1:p.Pro1142Thr
NM_001382802.1:c.3370C>A	NP_001369731.1:p.Pro1124Thr
NM_001382803.1:c.*207C>A	NP_001369732.1:n.*207C>A
NM_001382804.1:c.2800C>A	NP_001369733.1:p.Pro934Thr
NM_001382805.1:c.2677C>A	NP_001369734.1:p.Pro893Thr
NM_001382806.1:c.2590C>A	NP_001369735.1:p.Pro864Thr
NM_004448.4:c.3628C>A MANE Select	NP_004439.2:p.Pro1210Thr
NR_110535.2:n.3866C>A