Canonical Allele Identifier: CA2259228707

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727353C= , CM000679.2:g.39727353C=	GRCh38
NC_000017.10:g.37883606C= , CM000679.1:g.37883606C=	GRCh37
NC_000017.9:g.35137132C=	NCBI36
NG_007503.1:g.44214C= , LRG_724:g.44214C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3218C= MANE Select	ENSP00000269571.4:p.Ser1073=
ENST00000269571.9:c.3218C=	ENSP00000269571.4:p.Ser1073=
ENST00000406381.6:c.3128C=	ENSP00000385185.2:p.Ser1043=
ENST00000445658.6:c.2390C=	ENSP00000404047.2:p.Ser797=
ENST00000541774.5:c.3173C=	ENSP00000446466.1:p.Ser1058=
ENST00000578373.5:c.*3008C=	ENSP00000463427.1:n.*3008C=
ENST00000584450.5:c.3160-336C=	ENSP00000463714.1:n.3160-336C=
ENST00000584601.5:c.3128C=	ENSP00000462438.1:p.Ser1043=
NM_001005862.2:c.3128C= , LRG_724t1:c.3128C=	NP_001005862.1:p.Ser1043=
NM_001289936.1:c.3173C= , LRG_724t4:c.3173C=	NP_001276865.1:p.Ser1058=
NM_001289937.1:c.3160-336C=	NP_001276866.1:n.3160-336C=
NM_004448.3:c.3218C= , LRG_724t2:c.3218C=	NP_004439.2:p.Ser1073=
NR_110535.1:n.3542C=
XM_024450641.1:c.3356C=	XP_024306409.1:p.Ser1119=
XM_024450642.1:c.3311C=	XP_024306410.1:p.Ser1104=
XM_024450643.1:c.3266C=	XP_024306411.1:p.Ser1089=
NM_001005862.3:c.3128C=	NP_001005862.1:p.Ser1043=
NM_001289936.2:c.3173C=	NP_001276865.1:p.Ser1058=
NM_001289937.2:c.3160-336C=	NP_001276866.1:n.3160-336C=
NM_001382782.1:c.3128C=	NP_001369711.1:p.Ser1043=
NM_001382783.1:c.3128C=	NP_001369712.1:p.Ser1043=
NM_001382784.1:c.3335C=	NP_001369713.1:p.Ser1112=
NM_001382785.1:c.3320C=	NP_001369714.1:p.Ser1107=
NM_001382786.1:c.3299C=	NP_001369715.1:p.Ser1100=
NM_001382787.1:c.3293C=	NP_001369716.1:p.Ser1098=
NM_001382788.1:c.3248C=	NP_001369717.1:p.Ser1083=
NM_001382789.1:c.3239C=	NP_001369718.1:p.Ser1080=
NM_001382790.1:c.3215C=	NP_001369719.1:p.Ser1072=
NM_001382791.1:c.3209C=	NP_001369720.1:p.Ser1070=
NM_001382792.1:c.3182C=	NP_001369721.1:p.Ser1061=
NM_001382793.1:c.3176C=	NP_001369722.1:p.Ser1059=
NM_001382794.1:c.3176C=	NP_001369723.1:p.Ser1059=
NM_001382795.1:c.3170C=	NP_001369724.1:p.Ser1057=
NM_001382796.1:c.3131C=	NP_001369725.1:p.Ser1044=
NM_001382797.1:c.3119C=	NP_001369726.1:p.Ser1040=
NM_001382798.1:c.3062C=	NP_001369727.1:p.Ser1021=
NM_001382799.1:c.3038C=	NP_001369728.1:p.Ser1013=
NM_001382800.1:c.3032C=	NP_001369729.1:p.Ser1011=
NM_001382801.1:c.3014C=	NP_001369730.1:p.Ser1005=
NM_001382802.1:c.2960C=	NP_001369731.1:p.Ser987=
NM_001382803.1:c.3118-336C=	NP_001369732.1:n.3118-336C=
NM_001382804.1:c.2390C=	NP_001369733.1:p.Ser797=
NM_001382805.1:c.2267C=	NP_001369734.1:p.Ser756=
NM_001382806.1:c.2180C=	NP_001369735.1:p.Ser727=
NM_004448.4:c.3218C= MANE Select	NP_004439.2:p.Ser1073=
NR_110535.2:n.3456C=