Canonical Allele Identifier: CA399310262

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059831355
• MyVariant Identifiers: chr17:g.37883592G>C (hg19) ; chr17:g.39727339G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727339G>C , CM000679.2:g.39727339G>C	GRCh38
NC_000017.10:g.37883592G>C , CM000679.1:g.37883592G>C	GRCh37
NC_000017.9:g.35137118G>C	NCBI36
NG_007503.1:g.44200G>C , LRG_724:g.44200G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3204G>C MANE Select	ENSP00000269571.4:p.Glu1068Asp
ENST00000269571.9:c.3204G>C	ENSP00000269571.4:p.Glu1068Asp
ENST00000406381.6:c.3114G>C	ENSP00000385185.2:p.Glu1038Asp
ENST00000445658.6:c.2376G>C	ENSP00000404047.2:p.Glu792Asp
ENST00000541774.5:c.3159G>C	ENSP00000446466.1:p.Glu1053Asp
ENST00000578373.5:c.*2994G>C	ENSP00000463427.1:n.*2994G>C
ENST00000584450.5:c.3159+336G>C	ENSP00000463714.1:n.3159+336G>C
ENST00000584601.5:c.3114G>C	ENSP00000462438.1:p.Glu1038Asp
NM_001005862.2:c.3114G>C , LRG_724t1:c.3114G>C	NP_001005862.1:p.Glu1038Asp
NM_001289936.1:c.3159G>C , LRG_724t4:c.3159G>C	NP_001276865.1:p.Glu1053Asp
NM_001289937.1:c.3159+336G>C	NP_001276866.1:n.3159+336G>C
NM_004448.3:c.3204G>C , LRG_724t2:c.3204G>C	NP_004439.2:p.Glu1068Asp
NR_110535.1:n.3528G>C
XM_024450641.1:c.3342G>C	XP_024306409.1:p.Glu1114Asp
XM_024450642.1:c.3297G>C	XP_024306410.1:p.Glu1099Asp
XM_024450643.1:c.3252G>C	XP_024306411.1:p.Glu1084Asp
NM_001005862.3:c.3114G>C	NP_001005862.1:p.Glu1038Asp
NM_001289936.2:c.3159G>C	NP_001276865.1:p.Glu1053Asp
NM_001289937.2:c.3159+336G>C	NP_001276866.1:n.3159+336G>C
NM_001382782.1:c.3114G>C	NP_001369711.1:p.Glu1038Asp
NM_001382783.1:c.3114G>C	NP_001369712.1:p.Glu1038Asp
NM_001382784.1:c.3321G>C	NP_001369713.1:p.Glu1107Asp
NM_001382785.1:c.3306G>C	NP_001369714.1:p.Glu1102Asp
NM_001382786.1:c.3285G>C	NP_001369715.1:p.Glu1095Asp
NM_001382787.1:c.3279G>C	NP_001369716.1:p.Glu1093Asp
NM_001382788.1:c.3234G>C	NP_001369717.1:p.Glu1078Asp
NM_001382789.1:c.3225G>C	NP_001369718.1:p.Glu1075Asp
NM_001382790.1:c.3201G>C	NP_001369719.1:p.Glu1067Asp
NM_001382791.1:c.3195G>C	NP_001369720.1:p.Glu1065Asp
NM_001382792.1:c.3168G>C	NP_001369721.1:p.Glu1056Asp
NM_001382793.1:c.3162G>C	NP_001369722.1:p.Glu1054Asp
NM_001382794.1:c.3162G>C	NP_001369723.1:p.Glu1054Asp
NM_001382795.1:c.3156G>C	NP_001369724.1:p.Glu1052Asp
NM_001382796.1:c.3117G>C	NP_001369725.1:p.Glu1039Asp
NM_001382797.1:c.3105G>C	NP_001369726.1:p.Glu1035Asp
NM_001382798.1:c.3048G>C	NP_001369727.1:p.Glu1016Asp
NM_001382799.1:c.3024G>C	NP_001369728.1:p.Glu1008Asp
NM_001382800.1:c.3018G>C	NP_001369729.1:p.Glu1006Asp
NM_001382801.1:c.3000G>C	NP_001369730.1:p.Glu1000Asp
NM_001382802.1:c.2946G>C	NP_001369731.1:p.Glu982Asp
NM_001382803.1:c.3117+336G>C	NP_001369732.1:n.3117+336G>C
NM_001382804.1:c.2376G>C	NP_001369733.1:p.Glu792Asp
NM_001382805.1:c.2253G>C	NP_001369734.1:p.Glu751Asp
NM_001382806.1:c.2166G>C	NP_001369735.1:p.Glu722Asp
NM_004448.4:c.3204G>C MANE Select	NP_004439.2:p.Glu1068Asp
NR_110535.2:n.3442G>C