Canonical Allele Identifier: CA399314138

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143310445
• MyVariant Identifiers: chr17:g.37884163G>T (hg19) ; chr17:g.39727910G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727910G>T , CM000679.2:g.39727910G>T	GRCh38
NC_000017.10:g.37884163G>T , CM000679.1:g.37884163G>T	GRCh37
NC_000017.9:g.35137689G>T	NCBI36
NG_007503.1:g.44771G>T , LRG_724:g.44771G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3634G>T MANE Select	ENSP00000269571.4:p.Ala1212Ser
ENST00000269571.9:c.3634G>T	ENSP00000269571.4:p.Ala1212Ser
ENST00000406381.6:c.3544G>T	ENSP00000385185.2:p.Ala1182Ser
ENST00000445658.6:c.2806G>T	ENSP00000404047.2:p.Ala936Ser
ENST00000541774.5:c.3589G>T	ENSP00000446466.1:p.Ala1197Ser
ENST00000578373.5:c.*3424G>T	ENSP00000463427.1:n.*3424G>T
ENST00000584450.5:c.*213G>T	ENSP00000463714.1:n.*213G>T
ENST00000584601.5:c.3544G>T	ENSP00000462438.1:p.Ala1182Ser
NM_001005862.2:c.3544G>T , LRG_724t1:c.3544G>T	NP_001005862.1:p.Ala1182Ser
NM_001289936.1:c.3589G>T , LRG_724t4:c.3589G>T	NP_001276865.1:p.Ala1197Ser
NM_001289937.1:c.*213G>T	NP_001276866.1:n.*213G>T
NM_004448.3:c.3634G>T , LRG_724t2:c.3634G>T	NP_004439.2:p.Ala1212Ser
NR_110535.1:n.3958G>T
XM_024450641.1:c.3772G>T	XP_024306409.1:p.Ala1258Ser
XM_024450642.1:c.3727G>T	XP_024306410.1:p.Ala1243Ser
XM_024450643.1:c.3682G>T	XP_024306411.1:p.Ala1228Ser
NM_001005862.3:c.3544G>T	NP_001005862.1:p.Ala1182Ser
NM_001289936.2:c.3589G>T	NP_001276865.1:p.Ala1197Ser
NM_001289937.2:c.*213G>T	NP_001276866.1:n.*213G>T
NM_001382782.1:c.3544G>T	NP_001369711.1:p.Ala1182Ser
NM_001382783.1:c.3544G>T	NP_001369712.1:p.Ala1182Ser
NM_001382784.1:c.3751G>T	NP_001369713.1:p.Ala1251Ser
NM_001382785.1:c.3736G>T	NP_001369714.1:p.Ala1246Ser
NM_001382786.1:c.3715G>T	NP_001369715.1:p.Ala1239Ser
NM_001382787.1:c.3709G>T	NP_001369716.1:p.Ala1237Ser
NM_001382788.1:c.3664G>T	NP_001369717.1:p.Ala1222Ser
NM_001382789.1:c.3655G>T	NP_001369718.1:p.Ala1219Ser
NM_001382790.1:c.3631G>T	NP_001369719.1:p.Ala1211Ser
NM_001382791.1:c.3625G>T	NP_001369720.1:p.Ala1209Ser
NM_001382792.1:c.3598G>T	NP_001369721.1:p.Ala1200Ser
NM_001382793.1:c.3592G>T	NP_001369722.1:p.Ala1198Ser
NM_001382794.1:c.3592G>T	NP_001369723.1:p.Ala1198Ser
NM_001382795.1:c.3586G>T	NP_001369724.1:p.Ala1196Ser
NM_001382796.1:c.3547G>T	NP_001369725.1:p.Ala1183Ser
NM_001382797.1:c.3535G>T	NP_001369726.1:p.Ala1179Ser
NM_001382798.1:c.3478G>T	NP_001369727.1:p.Ala1160Ser
NM_001382799.1:c.3454G>T	NP_001369728.1:p.Ala1152Ser
NM_001382800.1:c.3448G>T	NP_001369729.1:p.Ala1150Ser
NM_001382801.1:c.3430G>T	NP_001369730.1:p.Ala1144Ser
NM_001382802.1:c.3376G>T	NP_001369731.1:p.Ala1126Ser
NM_001382803.1:c.*213G>T	NP_001369732.1:n.*213G>T
NM_001382804.1:c.2806G>T	NP_001369733.1:p.Ala936Ser
NM_001382805.1:c.2683G>T	NP_001369734.1:p.Ala895Ser
NM_001382806.1:c.2596G>T	NP_001369735.1:p.Ala866Ser
NM_004448.4:c.3634G>T MANE Select	NP_004439.2:p.Ala1212Ser
NR_110535.2:n.3872G>T