Canonical Allele Identifier: CA2259229288

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727844G= , CM000679.2:g.39727844G=	GRCh38
NC_000017.10:g.37884097G= , CM000679.1:g.37884097G=	GRCh37
NC_000017.9:g.35137623G=	NCBI36
NG_007503.1:g.44705G= , LRG_724:g.44705G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3568G= MANE Select	ENSP00000269571.4:p.Ala1190=
ENST00000269571.9:c.3568G=	ENSP00000269571.4:p.Ala1190=
ENST00000406381.6:c.3478G=	ENSP00000385185.2:p.Ala1160=
ENST00000445658.6:c.2740G=	ENSP00000404047.2:p.Ala914=
ENST00000541774.5:c.3523G=	ENSP00000446466.1:p.Ala1175=
ENST00000578373.5:c.*3358G=	ENSP00000463427.1:n.*3358G=
ENST00000584450.5:c.*147G=	ENSP00000463714.1:n.*147G=
ENST00000584601.5:c.3478G=	ENSP00000462438.1:p.Ala1160=
NM_001005862.2:c.3478G= , LRG_724t1:c.3478G=	NP_001005862.1:p.Ala1160=
NM_001289936.1:c.3523G= , LRG_724t4:c.3523G=	NP_001276865.1:p.Ala1175=
NM_001289937.1:c.*147G=	NP_001276866.1:n.*147G=
NM_004448.3:c.3568G= , LRG_724t2:c.3568G=	NP_004439.2:p.Ala1190=
NR_110535.1:n.3892G=
XM_024450641.1:c.3706G=	XP_024306409.1:p.Ala1236=
XM_024450642.1:c.3661G=	XP_024306410.1:p.Ala1221=
XM_024450643.1:c.3616G=	XP_024306411.1:p.Ala1206=
NM_001005862.3:c.3478G=	NP_001005862.1:p.Ala1160=
NM_001289936.2:c.3523G=	NP_001276865.1:p.Ala1175=
NM_001289937.2:c.*147G=	NP_001276866.1:n.*147G=
NM_001382782.1:c.3478G=	NP_001369711.1:p.Ala1160=
NM_001382783.1:c.3478G=	NP_001369712.1:p.Ala1160=
NM_001382784.1:c.3685G=	NP_001369713.1:p.Ala1229=
NM_001382785.1:c.3670G=	NP_001369714.1:p.Ala1224=
NM_001382786.1:c.3649G=	NP_001369715.1:p.Ala1217=
NM_001382787.1:c.3643G=	NP_001369716.1:p.Ala1215=
NM_001382788.1:c.3598G=	NP_001369717.1:p.Ala1200=
NM_001382789.1:c.3589G=	NP_001369718.1:p.Ala1197=
NM_001382790.1:c.3565G=	NP_001369719.1:p.Ala1189=
NM_001382791.1:c.3559G=	NP_001369720.1:p.Ala1187=
NM_001382792.1:c.3532G=	NP_001369721.1:p.Ala1178=
NM_001382793.1:c.3526G=	NP_001369722.1:p.Ala1176=
NM_001382794.1:c.3526G=	NP_001369723.1:p.Ala1176=
NM_001382795.1:c.3520G=	NP_001369724.1:p.Ala1174=
NM_001382796.1:c.3481G=	NP_001369725.1:p.Ala1161=
NM_001382797.1:c.3469G=	NP_001369726.1:p.Ala1157=
NM_001382798.1:c.3412G=	NP_001369727.1:p.Ala1138=
NM_001382799.1:c.3388G=	NP_001369728.1:p.Ala1130=
NM_001382800.1:c.3382G=	NP_001369729.1:p.Ala1128=
NM_001382801.1:c.3364G=	NP_001369730.1:p.Ala1122=
NM_001382802.1:c.3310G=	NP_001369731.1:p.Ala1104=
NM_001382803.1:c.*147G=	NP_001369732.1:n.*147G=
NM_001382804.1:c.2740G=	NP_001369733.1:p.Ala914=
NM_001382805.1:c.2617G=	NP_001369734.1:p.Ala873=
NM_001382806.1:c.2530G=	NP_001369735.1:p.Ala844=
NM_004448.4:c.3568G= MANE Select	NP_004439.2:p.Ala1190=
NR_110535.2:n.3806G=