Canonical Allele Identifier: CA2259228808

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727445C= , CM000679.2:g.39727445C=	GRCh38
NC_000017.10:g.37883698C= , CM000679.1:g.37883698C=	GRCh37
NC_000017.9:g.35137224C=	NCBI36
NG_007503.1:g.44306C= , LRG_724:g.44306C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3310C= MANE Select	ENSP00000269571.4:p.His1104=
ENST00000269571.9:c.3310C=	ENSP00000269571.4:p.His1104=
ENST00000406381.6:c.3220C=	ENSP00000385185.2:p.His1074=
ENST00000445658.6:c.2482C=	ENSP00000404047.2:p.His828=
ENST00000541774.5:c.3265C=	ENSP00000446466.1:p.His1089=
ENST00000578373.5:c.*3100C=	ENSP00000463427.1:n.*3100C=
ENST00000584450.5:c.3160-244C=	ENSP00000463714.1:n.3160-244C=
ENST00000584601.5:c.3220C=	ENSP00000462438.1:p.His1074=
NM_001005862.2:c.3220C= , LRG_724t1:c.3220C=	NP_001005862.1:p.His1074=
NM_001289936.1:c.3265C= , LRG_724t4:c.3265C=	NP_001276865.1:p.His1089=
NM_001289937.1:c.3160-244C=	NP_001276866.1:n.3160-244C=
NM_004448.3:c.3310C= , LRG_724t2:c.3310C=	NP_004439.2:p.His1104=
NR_110535.1:n.3634C=
XM_024450641.1:c.3448C=	XP_024306409.1:p.His1150=
XM_024450642.1:c.3403C=	XP_024306410.1:p.His1135=
XM_024450643.1:c.3358C=	XP_024306411.1:p.His1120=
NM_001005862.3:c.3220C=	NP_001005862.1:p.His1074=
NM_001289936.2:c.3265C=	NP_001276865.1:p.His1089=
NM_001289937.2:c.3160-244C=	NP_001276866.1:n.3160-244C=
NM_001382782.1:c.3220C=	NP_001369711.1:p.His1074=
NM_001382783.1:c.3220C=	NP_001369712.1:p.His1074=
NM_001382784.1:c.3427C=	NP_001369713.1:p.His1143=
NM_001382785.1:c.3412C=	NP_001369714.1:p.His1138=
NM_001382786.1:c.3391C=	NP_001369715.1:p.His1131=
NM_001382787.1:c.3385C=	NP_001369716.1:p.His1129=
NM_001382788.1:c.3340C=	NP_001369717.1:p.His1114=
NM_001382789.1:c.3331C=	NP_001369718.1:p.His1111=
NM_001382790.1:c.3307C=	NP_001369719.1:p.His1103=
NM_001382791.1:c.3301C=	NP_001369720.1:p.His1101=
NM_001382792.1:c.3274C=	NP_001369721.1:p.His1092=
NM_001382793.1:c.3268C=	NP_001369722.1:p.His1090=
NM_001382794.1:c.3268C=	NP_001369723.1:p.His1090=
NM_001382795.1:c.3262C=	NP_001369724.1:p.His1088=
NM_001382796.1:c.3223C=	NP_001369725.1:p.His1075=
NM_001382797.1:c.3211C=	NP_001369726.1:p.His1071=
NM_001382798.1:c.3154C=	NP_001369727.1:p.His1052=
NM_001382799.1:c.3130C=	NP_001369728.1:p.His1044=
NM_001382800.1:c.3124C=	NP_001369729.1:p.His1042=
NM_001382801.1:c.3106C=	NP_001369730.1:p.His1036=
NM_001382802.1:c.3052C=	NP_001369731.1:p.His1018=
NM_001382803.1:c.3118-244C=	NP_001369732.1:n.3118-244C=
NM_001382804.1:c.2482C=	NP_001369733.1:p.His828=
NM_001382805.1:c.2359C=	NP_001369734.1:p.His787=
NM_001382806.1:c.2272C=	NP_001369735.1:p.His758=
NM_004448.4:c.3310C= MANE Select	NP_004439.2:p.His1104=
NR_110535.2:n.3548C=