Canonical Allele Identifier: CA399302955

Gene: ERBB2

Linked Data

• dbSNP Id: rs751226373
• MyVariant Identifiers: chr17:g.37881022G>C (hg19) ; chr17:g.39724769G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724769G>C , CM000679.2:g.39724769G>C	GRCh38
NC_000017.10:g.37881022G>C , CM000679.1:g.37881022G>C	GRCh37
NC_000017.9:g.35134548G>C	NCBI36
NG_007503.1:g.41630G>C , LRG_724:g.41630G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2351G>C MANE Select	ENSP00000269571.4:p.Arg784Pro
ENST00000269571.9:c.2351G>C	ENSP00000269571.4:p.Arg784Pro
ENST00000406381.6:c.2261G>C	ENSP00000385185.2:p.Arg754Pro
ENST00000445658.6:c.1523G>C	ENSP00000404047.2:p.Arg508Pro
ENST00000541774.5:c.2306G>C	ENSP00000446466.1:p.Arg769Pro
ENST00000578373.5:c.*2141G>C	ENSP00000463427.1:n.*2141G>C
ENST00000580074.1:c.457G>C
ENST00000583038.5:n.3485G>C
ENST00000584450.5:c.2351G>C	ENSP00000463714.1:p.Arg784Pro
ENST00000584601.5:c.2261G>C	ENSP00000462438.1:p.Arg754Pro
NM_001005862.2:c.2261G>C , LRG_724t1:c.2261G>C	NP_001005862.1:p.Arg754Pro
NM_001289936.1:c.2306G>C , LRG_724t4:c.2306G>C	NP_001276865.1:p.Arg769Pro
NM_001289937.1:c.2351G>C	NP_001276866.1:p.Arg784Pro
NM_004448.3:c.2351G>C , LRG_724t2:c.2351G>C	NP_004439.2:p.Arg784Pro
NR_110535.1:n.2675G>C
XM_024450641.1:c.2489G>C	XP_024306409.1:p.Arg830Pro
XM_024450642.1:c.2444G>C	XP_024306410.1:p.Arg815Pro
XM_024450643.1:c.2399G>C	XP_024306411.1:p.Arg800Pro
NM_001005862.3:c.2261G>C	NP_001005862.1:p.Arg754Pro
NM_001289936.2:c.2306G>C	NP_001276865.1:p.Arg769Pro
NM_001289937.2:c.2351G>C	NP_001276866.1:p.Arg784Pro
NM_001382782.1:c.2261G>C	NP_001369711.1:p.Arg754Pro
NM_001382783.1:c.2261G>C	NP_001369712.1:p.Arg754Pro
NM_001382784.1:c.2468G>C	NP_001369713.1:p.Arg823Pro
NM_001382785.1:c.2453G>C	NP_001369714.1:p.Arg818Pro
NM_001382786.1:c.2432G>C	NP_001369715.1:p.Arg811Pro
NM_001382787.1:c.2426G>C	NP_001369716.1:p.Arg809Pro
NM_001382788.1:c.2381G>C	NP_001369717.1:p.Arg794Pro
NM_001382789.1:c.2372G>C	NP_001369718.1:p.Arg791Pro
NM_001382790.1:c.2348G>C	NP_001369719.1:p.Arg783Pro
NM_001382791.1:c.2342G>C	NP_001369720.1:p.Arg781Pro
NM_001382792.1:c.2315G>C	NP_001369721.1:p.Arg772Pro
NM_001382793.1:c.2309G>C	NP_001369722.1:p.Arg770Pro
NM_001382794.1:c.2309G>C	NP_001369723.1:p.Arg770Pro
NM_001382795.1:c.2303G>C	NP_001369724.1:p.Arg768Pro
NM_001382796.1:c.2351G>C	NP_001369725.1:p.Arg784Pro
NM_001382797.1:c.2252G>C	NP_001369726.1:p.Arg751Pro
NM_001382798.1:c.2351G>C	NP_001369727.1:p.Arg784Pro
NM_001382799.1:c.2171G>C	NP_001369728.1:p.Arg724Pro
NM_001382800.1:c.2308-280G>C	NP_001369729.1:n.2308-280G>C
NM_001382801.1:c.2303G>C	NP_001369730.1:p.Arg768Pro
NM_001382802.1:c.2093G>C	NP_001369731.1:p.Arg698Pro
NM_001382803.1:c.2309G>C	NP_001369732.1:p.Arg770Pro
NM_001382804.1:c.1523G>C	NP_001369733.1:p.Arg508Pro
NM_001382805.1:c.2208+1109G>C	NP_001369734.1:n.2208+1109G>C
NM_001382806.1:c.1313G>C	NP_001369735.1:p.Arg438Pro
NM_004448.4:c.2351G>C MANE Select	NP_004439.2:p.Arg784Pro
NR_110535.2:n.2589G>C