Canonical Allele Identifier: CA399314093

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059869654
• COSMIC: COSM1710191
• MyVariant Identifiers: chr17:g.37884157C>T (hg19) ; chr17:g.39727904C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3628C>T MANE Select	ENSP00000269571.4:p.Pro1210Ser
ENST00000269571.9:c.3628C>T	ENSP00000269571.4:p.Pro1210Ser
ENST00000406381.6:c.3538C>T	ENSP00000385185.2:p.Pro1180Ser
ENST00000445658.6:c.2800C>T	ENSP00000404047.2:p.Pro934Ser
ENST00000541774.5:c.3583C>T	ENSP00000446466.1:p.Pro1195Ser
ENST00000578373.5:c.*3418C>T	ENSP00000463427.1:n.*3418C>T
ENST00000584450.5:c.*207C>T	ENSP00000463714.1:n.*207C>T
ENST00000584601.5:c.3538C>T	ENSP00000462438.1:p.Pro1180Ser
NM_001005862.2:c.3538C>T , LRG_724t1:c.3538C>T	NP_001005862.1:p.Pro1180Ser
NM_001289936.1:c.3583C>T , LRG_724t4:c.3583C>T	NP_001276865.1:p.Pro1195Ser
NM_001289937.1:c.*207C>T	NP_001276866.1:n.*207C>T
NM_004448.3:c.3628C>T , LRG_724t2:c.3628C>T	NP_004439.2:p.Pro1210Ser
NR_110535.1:n.3952C>T
XM_024450641.1:c.3766C>T	XP_024306409.1:p.Pro1256Ser
XM_024450642.1:c.3721C>T	XP_024306410.1:p.Pro1241Ser
XM_024450643.1:c.3676C>T	XP_024306411.1:p.Pro1226Ser
NM_001005862.3:c.3538C>T	NP_001005862.1:p.Pro1180Ser
NM_001289936.2:c.3583C>T	NP_001276865.1:p.Pro1195Ser
NM_001289937.2:c.*207C>T	NP_001276866.1:n.*207C>T
NM_001382782.1:c.3538C>T	NP_001369711.1:p.Pro1180Ser
NM_001382783.1:c.3538C>T	NP_001369712.1:p.Pro1180Ser
NM_001382784.1:c.3745C>T	NP_001369713.1:p.Pro1249Ser
NM_001382785.1:c.3730C>T	NP_001369714.1:p.Pro1244Ser
NM_001382786.1:c.3709C>T	NP_001369715.1:p.Pro1237Ser
NM_001382787.1:c.3703C>T	NP_001369716.1:p.Pro1235Ser
NM_001382788.1:c.3658C>T	NP_001369717.1:p.Pro1220Ser
NM_001382789.1:c.3649C>T	NP_001369718.1:p.Pro1217Ser
NM_001382790.1:c.3625C>T	NP_001369719.1:p.Pro1209Ser
NM_001382791.1:c.3619C>T	NP_001369720.1:p.Pro1207Ser
NM_001382792.1:c.3592C>T	NP_001369721.1:p.Pro1198Ser
NM_001382793.1:c.3586C>T	NP_001369722.1:p.Pro1196Ser
NM_001382794.1:c.3586C>T	NP_001369723.1:p.Pro1196Ser
NM_001382795.1:c.3580C>T	NP_001369724.1:p.Pro1194Ser
NM_001382796.1:c.3541C>T	NP_001369725.1:p.Pro1181Ser
NM_001382797.1:c.3529C>T	NP_001369726.1:p.Pro1177Ser
NM_001382798.1:c.3472C>T	NP_001369727.1:p.Pro1158Ser
NM_001382799.1:c.3448C>T	NP_001369728.1:p.Pro1150Ser
NM_001382800.1:c.3442C>T	NP_001369729.1:p.Pro1148Ser
NM_001382801.1:c.3424C>T	NP_001369730.1:p.Pro1142Ser
NM_001382802.1:c.3370C>T	NP_001369731.1:p.Pro1124Ser
NM_001382803.1:c.*207C>T	NP_001369732.1:n.*207C>T
NM_001382804.1:c.2800C>T	NP_001369733.1:p.Pro934Ser
NM_001382805.1:c.2677C>T	NP_001369734.1:p.Pro893Ser
NM_001382806.1:c.2590C>T	NP_001369735.1:p.Pro864Ser
NM_004448.4:c.3628C>T MANE Select	NP_004439.2:p.Pro1210Ser
NR_110535.2:n.3866C>T