Canonical Allele Identifier: CA2259228681

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727336A= , CM000679.2:g.39727336A=	GRCh38
NC_000017.10:g.37883589A= , CM000679.1:g.37883589A=	GRCh37
NC_000017.9:g.35137115A=	NCBI36
NG_007503.1:g.44197A= , LRG_724:g.44197A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3201A= MANE Select	ENSP00000269571.4:p.Glu1067=
ENST00000269571.9:c.3201A=	ENSP00000269571.4:p.Glu1067=
ENST00000406381.6:c.3111A=	ENSP00000385185.2:p.Glu1037=
ENST00000445658.6:c.2373A=	ENSP00000404047.2:p.Glu791=
ENST00000541774.5:c.3156A=	ENSP00000446466.1:p.Glu1052=
ENST00000578373.5:c.*2991A=	ENSP00000463427.1:n.*2991A=
ENST00000584450.5:c.3159+333A=	ENSP00000463714.1:n.3159+333A=
ENST00000584601.5:c.3111A=	ENSP00000462438.1:p.Glu1037=
NM_001005862.2:c.3111A= , LRG_724t1:c.3111A=	NP_001005862.1:p.Glu1037=
NM_001289936.1:c.3156A= , LRG_724t4:c.3156A=	NP_001276865.1:p.Glu1052=
NM_001289937.1:c.3159+333A=	NP_001276866.1:n.3159+333A=
NM_004448.3:c.3201A= , LRG_724t2:c.3201A=	NP_004439.2:p.Glu1067=
NR_110535.1:n.3525A=
XM_024450641.1:c.3339A=	XP_024306409.1:p.Glu1113=
XM_024450642.1:c.3294A=	XP_024306410.1:p.Glu1098=
XM_024450643.1:c.3249A=	XP_024306411.1:p.Glu1083=
NM_001005862.3:c.3111A=	NP_001005862.1:p.Glu1037=
NM_001289936.2:c.3156A=	NP_001276865.1:p.Glu1052=
NM_001289937.2:c.3159+333A=	NP_001276866.1:n.3159+333A=
NM_001382782.1:c.3111A=	NP_001369711.1:p.Glu1037=
NM_001382783.1:c.3111A=	NP_001369712.1:p.Glu1037=
NM_001382784.1:c.3318A=	NP_001369713.1:p.Glu1106=
NM_001382785.1:c.3303A=	NP_001369714.1:p.Glu1101=
NM_001382786.1:c.3282A=	NP_001369715.1:p.Glu1094=
NM_001382787.1:c.3276A=	NP_001369716.1:p.Glu1092=
NM_001382788.1:c.3231A=	NP_001369717.1:p.Glu1077=
NM_001382789.1:c.3222A=	NP_001369718.1:p.Glu1074=
NM_001382790.1:c.3198A=	NP_001369719.1:p.Glu1066=
NM_001382791.1:c.3192A=	NP_001369720.1:p.Glu1064=
NM_001382792.1:c.3165A=	NP_001369721.1:p.Glu1055=
NM_001382793.1:c.3159A=	NP_001369722.1:p.Glu1053=
NM_001382794.1:c.3159A=	NP_001369723.1:p.Glu1053=
NM_001382795.1:c.3153A=	NP_001369724.1:p.Glu1051=
NM_001382796.1:c.3114A=	NP_001369725.1:p.Glu1038=
NM_001382797.1:c.3102A=	NP_001369726.1:p.Glu1034=
NM_001382798.1:c.3045A=	NP_001369727.1:p.Glu1015=
NM_001382799.1:c.3021A=	NP_001369728.1:p.Glu1007=
NM_001382800.1:c.3015A=	NP_001369729.1:p.Glu1005=
NM_001382801.1:c.2997A=	NP_001369730.1:p.Glu999=
NM_001382802.1:c.2943A=	NP_001369731.1:p.Glu981=
NM_001382803.1:c.3117+333A=	NP_001369732.1:n.3117+333A=
NM_001382804.1:c.2373A=	NP_001369733.1:p.Glu791=
NM_001382805.1:c.2250A=	NP_001369734.1:p.Glu750=
NM_001382806.1:c.2163A=	NP_001369735.1:p.Glu721=
NM_004448.4:c.3201A= MANE Select	NP_004439.2:p.Glu1067=
NR_110535.2:n.3439A=