Canonical Allele Identifier: CA2259229144

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727522C= , CM000679.2:g.39727522C=	GRCh38
NC_000017.10:g.37883775C= , CM000679.1:g.37883775C=	GRCh37
NC_000017.9:g.35137301C=	NCBI36
NG_007503.1:g.44383C= , LRG_724:g.44383C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3387C= MANE Select	ENSP00000269571.4:p.Ala1129=
ENST00000269571.9:c.3387C=	ENSP00000269571.4:p.Ala1129=
ENST00000406381.6:c.3297C=	ENSP00000385185.2:p.Ala1099=
ENST00000445658.6:c.2559C=	ENSP00000404047.2:p.Ala853=
ENST00000541774.5:c.3342C=	ENSP00000446466.1:p.Ala1114=
ENST00000578373.5:c.*3177C=	ENSP00000463427.1:n.*3177C=
ENST00000584450.5:c.3160-167C=	ENSP00000463714.1:n.3160-167C=
ENST00000584601.5:c.3297C=	ENSP00000462438.1:p.Ala1099=
NM_001005862.2:c.3297C= , LRG_724t1:c.3297C=	NP_001005862.1:p.Ala1099=
NM_001289936.1:c.3342C= , LRG_724t4:c.3342C=	NP_001276865.1:p.Ala1114=
NM_001289937.1:c.3160-167C=	NP_001276866.1:n.3160-167C=
NM_004448.3:c.3387C= , LRG_724t2:c.3387C=	NP_004439.2:p.Ala1129=
NR_110535.1:n.3711C=
XM_024450641.1:c.3525C=	XP_024306409.1:p.Ala1175=
XM_024450642.1:c.3480C=	XP_024306410.1:p.Ala1160=
XM_024450643.1:c.3435C=	XP_024306411.1:p.Ala1145=
NM_001005862.3:c.3297C=	NP_001005862.1:p.Ala1099=
NM_001289936.2:c.3342C=	NP_001276865.1:p.Ala1114=
NM_001289937.2:c.3160-167C=	NP_001276866.1:n.3160-167C=
NM_001382782.1:c.3297C=	NP_001369711.1:p.Ala1099=
NM_001382783.1:c.3297C=	NP_001369712.1:p.Ala1099=
NM_001382784.1:c.3504C=	NP_001369713.1:p.Ala1168=
NM_001382785.1:c.3489C=	NP_001369714.1:p.Ala1163=
NM_001382786.1:c.3468C=	NP_001369715.1:p.Ala1156=
NM_001382787.1:c.3462C=	NP_001369716.1:p.Ala1154=
NM_001382788.1:c.3417C=	NP_001369717.1:p.Ala1139=
NM_001382789.1:c.3408C=	NP_001369718.1:p.Ala1136=
NM_001382790.1:c.3384C=	NP_001369719.1:p.Ala1128=
NM_001382791.1:c.3378C=	NP_001369720.1:p.Ala1126=
NM_001382792.1:c.3351C=	NP_001369721.1:p.Ala1117=
NM_001382793.1:c.3345C=	NP_001369722.1:p.Ala1115=
NM_001382794.1:c.3345C=	NP_001369723.1:p.Ala1115=
NM_001382795.1:c.3339C=	NP_001369724.1:p.Ala1113=
NM_001382796.1:c.3300C=	NP_001369725.1:p.Ala1100=
NM_001382797.1:c.3288C=	NP_001369726.1:p.Ala1096=
NM_001382798.1:c.3231C=	NP_001369727.1:p.Ala1077=
NM_001382799.1:c.3207C=	NP_001369728.1:p.Ala1069=
NM_001382800.1:c.3201C=	NP_001369729.1:p.Ala1067=
NM_001382801.1:c.3183C=	NP_001369730.1:p.Ala1061=
NM_001382802.1:c.3129C=	NP_001369731.1:p.Ala1043=
NM_001382803.1:c.3118-167C=	NP_001369732.1:n.3118-167C=
NM_001382804.1:c.2559C=	NP_001369733.1:p.Ala853=
NM_001382805.1:c.2436C=	NP_001369734.1:p.Ala812=
NM_001382806.1:c.2349C=	NP_001369735.1:p.Ala783=
NM_004448.4:c.3387C= MANE Select	NP_004439.2:p.Ala1129=
NR_110535.2:n.3625C=