Canonical Allele Identifier: CA8533961

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39715744G>A , CM000679.2:g.39715744G>A	GRCh38
NC_000017.10:g.37871997G>A , CM000679.1:g.37871997G>A	GRCh37
NC_000017.9:g.35125523G>A	NCBI36
NG_007503.1:g.32605G>A , LRG_724:g.32605G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.1318G>A MANE Select	ENSP00000269571.4:p.Ala440Thr
ENST00000269571.9:c.1318G>A	ENSP00000269571.4:p.Ala440Thr
ENST00000406381.6:c.1228G>A	ENSP00000385185.2:p.Ala410Thr
ENST00000445658.6:c.490G>A	ENSP00000404047.2:p.Ala164Thr
ENST00000541774.5:c.1273G>A	ENSP00000446466.1:p.Ala425Thr
ENST00000578199.5:c.1228G>A	ENSP00000462808.1:p.Ala410Thr
ENST00000578373.5:c.*1108G>A	ENSP00000463427.1:n.*1108G>A
ENST00000582648.5:c.*351G>A	ENSP00000462024.1:n.*351G>A
ENST00000582788.5:n.807G>A
ENST00000583038.5:n.2010G>A
ENST00000584450.5:c.1318G>A	ENSP00000463714.1:p.Ala440Thr
ENST00000584601.5:c.1228G>A	ENSP00000462438.1:p.Ala410Thr
NM_001005862.2:c.1228G>A , LRG_724t1:c.1228G>A	NP_001005862.1:p.Ala410Thr
NM_001289936.1:c.1273G>A , LRG_724t4:c.1273G>A	NP_001276865.1:p.Ala425Thr
NM_001289937.1:c.1318G>A	NP_001276866.1:p.Ala440Thr
NM_001289938.1:c.1228G>A , LRG_724t3:c.1228G>A	NP_001276867.1:p.Ala410Thr
NM_004448.3:c.1318G>A , LRG_724t2:c.1318G>A	NP_004439.2:p.Ala440Thr
NR_110535.1:n.1642G>A
XM_024450641.1:c.1456G>A	XP_024306409.1:p.Ala486Thr
XM_024450642.1:c.1411G>A	XP_024306410.1:p.Ala471Thr
XM_024450643.1:c.1366G>A	XP_024306411.1:p.Ala456Thr
NM_001005862.3:c.1228G>A	NP_001005862.1:p.Ala410Thr
NM_001289936.2:c.1273G>A	NP_001276865.1:p.Ala425Thr
NM_001289937.2:c.1318G>A	NP_001276866.1:p.Ala440Thr
NM_001289938.2:c.1228G>A	NP_001276867.1:p.Ala410Thr
NM_001382782.1:c.1228G>A	NP_001369711.1:p.Ala410Thr
NM_001382783.1:c.1228G>A	NP_001369712.1:p.Ala410Thr
NM_001382784.1:c.1435G>A	NP_001369713.1:p.Ala479Thr
NM_001382785.1:c.1318G>A	NP_001369714.1:p.Ala440Thr
NM_001382786.1:c.1435G>A	NP_001369715.1:p.Ala479Thr
NM_001382787.1:c.1393G>A	NP_001369716.1:p.Ala465Thr
NM_001382788.1:c.1318G>A	NP_001369717.1:p.Ala440Thr
NM_001382789.1:c.1339G>A	NP_001369718.1:p.Ala447Thr
NM_001382790.1:c.1318G>A	NP_001369719.1:p.Ala440Thr
NM_001382791.1:c.1309G>A	NP_001369720.1:p.Ala437Thr
NM_001382792.1:c.1318G>A	NP_001369721.1:p.Ala440Thr
NM_001382793.1:c.1318G>A	NP_001369722.1:p.Ala440Thr
NM_001382794.1:c.1318G>A	NP_001369723.1:p.Ala440Thr
NM_001382795.1:c.1318G>A	NP_001369724.1:p.Ala440Thr
NM_001382796.1:c.1318G>A	NP_001369725.1:p.Ala440Thr
NM_001382797.1:c.1318G>A	NP_001369726.1:p.Ala440Thr
NM_001382798.1:c.1318G>A	NP_001369727.1:p.Ala440Thr
NM_001382799.1:c.1138G>A	NP_001369728.1:p.Ala380Thr
NM_001382800.1:c.1318G>A	NP_001369729.1:p.Ala440Thr
NM_001382801.1:c.1318G>A	NP_001369730.1:p.Ala440Thr
NM_001382802.1:c.1060G>A	NP_001369731.1:p.Ala354Thr
NM_001382803.1:c.1318G>A	NP_001369732.1:p.Ala440Thr
NM_001382804.1:c.490G>A	NP_001369733.1:p.Ala164Thr
NM_001382805.1:c.1318G>A	NP_001369734.1:p.Ala440Thr
NM_001382806.1:c.1222+385G>A	NP_001369735.1:n.1222+385G>A
NM_004448.4:c.1318G>A MANE Select	NP_004439.2:p.Ala440Thr
NR_110535.2:n.1556G>A