Canonical Allele Identifier: CA2259229231

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727724C= , CM000679.2:g.39727724C=	GRCh38
NC_000017.10:g.37883977C= , CM000679.1:g.37883977C=	GRCh37
NC_000017.9:g.35137503C=	NCBI36
NG_007503.1:g.44585C= , LRG_724:g.44585C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3448C= MANE Select	ENSP00000269571.4:p.Pro1150=
ENST00000269571.9:c.3448C=	ENSP00000269571.4:p.Pro1150=
ENST00000406381.6:c.3358C=	ENSP00000385185.2:p.Pro1120=
ENST00000445658.6:c.2620C=	ENSP00000404047.2:p.Pro874=
ENST00000541774.5:c.3403C=	ENSP00000446466.1:p.Pro1135=
ENST00000578373.5:c.*3238C=	ENSP00000463427.1:n.*3238C=
ENST00000584450.5:c.*27C=	ENSP00000463714.1:n.*27C=
ENST00000584601.5:c.3358C=	ENSP00000462438.1:p.Pro1120=
NM_001005862.2:c.3358C= , LRG_724t1:c.3358C=	NP_001005862.1:p.Pro1120=
NM_001289936.1:c.3403C= , LRG_724t4:c.3403C=	NP_001276865.1:p.Pro1135=
NM_001289937.1:c.*27C=	NP_001276866.1:n.*27C=
NM_004448.3:c.3448C= , LRG_724t2:c.3448C=	NP_004439.2:p.Pro1150=
NR_110535.1:n.3772C=
XM_024450641.1:c.3586C=	XP_024306409.1:p.Pro1196=
XM_024450642.1:c.3541C=	XP_024306410.1:p.Pro1181=
XM_024450643.1:c.3496C=	XP_024306411.1:p.Pro1166=
NM_001005862.3:c.3358C=	NP_001005862.1:p.Pro1120=
NM_001289936.2:c.3403C=	NP_001276865.1:p.Pro1135=
NM_001289937.2:c.*27C=	NP_001276866.1:n.*27C=
NM_001382782.1:c.3358C=	NP_001369711.1:p.Pro1120=
NM_001382783.1:c.3358C=	NP_001369712.1:p.Pro1120=
NM_001382784.1:c.3565C=	NP_001369713.1:p.Pro1189=
NM_001382785.1:c.3550C=	NP_001369714.1:p.Pro1184=
NM_001382786.1:c.3529C=	NP_001369715.1:p.Pro1177=
NM_001382787.1:c.3523C=	NP_001369716.1:p.Pro1175=
NM_001382788.1:c.3478C=	NP_001369717.1:p.Pro1160=
NM_001382789.1:c.3469C=	NP_001369718.1:p.Pro1157=
NM_001382790.1:c.3445C=	NP_001369719.1:p.Pro1149=
NM_001382791.1:c.3439C=	NP_001369720.1:p.Pro1147=
NM_001382792.1:c.3412C=	NP_001369721.1:p.Pro1138=
NM_001382793.1:c.3406C=	NP_001369722.1:p.Pro1136=
NM_001382794.1:c.3406C=	NP_001369723.1:p.Pro1136=
NM_001382795.1:c.3400C=	NP_001369724.1:p.Pro1134=
NM_001382796.1:c.3361C=	NP_001369725.1:p.Pro1121=
NM_001382797.1:c.3349C=	NP_001369726.1:p.Pro1117=
NM_001382798.1:c.3292C=	NP_001369727.1:p.Pro1098=
NM_001382799.1:c.3268C=	NP_001369728.1:p.Pro1090=
NM_001382800.1:c.3262C=	NP_001369729.1:p.Pro1088=
NM_001382801.1:c.3244C=	NP_001369730.1:p.Pro1082=
NM_001382802.1:c.3190C=	NP_001369731.1:p.Pro1064=
NM_001382803.1:c.*27C=	NP_001369732.1:n.*27C=
NM_001382804.1:c.2620C=	NP_001369733.1:p.Pro874=
NM_001382805.1:c.2497C=	NP_001369734.1:p.Pro833=
NM_001382806.1:c.2410C=	NP_001369735.1:p.Pro804=
NM_004448.4:c.3448C= MANE Select	NP_004439.2:p.Pro1150=
NR_110535.2:n.3686C=