Canonical Allele Identifier: CA399304356

Gene: ERBB2

Linked Data

• dbSNP Id: rs1422047458
• MyVariant Identifiers: chr17:g.37881340G>T (hg19) ; chr17:g.39725087G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725087G>T , CM000679.2:g.39725087G>T	GRCh38
NC_000017.10:g.37881340G>T , CM000679.1:g.37881340G>T	GRCh37
NC_000017.9:g.35134866G>T	NCBI36
NG_007503.1:g.41948G>T , LRG_724:g.41948G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2532G>T MANE Select	ENSP00000269571.4:p.Arg844Ser
ENST00000269571.9:c.2532G>T	ENSP00000269571.4:p.Arg844Ser
ENST00000406381.6:c.2442G>T	ENSP00000385185.2:p.Arg814Ser
ENST00000445658.6:c.1704G>T	ENSP00000404047.2:p.Arg568Ser
ENST00000541774.5:c.2487G>T	ENSP00000446466.1:p.Arg829Ser
ENST00000578373.5:c.*2322G>T	ENSP00000463427.1:n.*2322G>T
ENST00000580074.1:c.638G>T
ENST00000583038.5:n.3666G>T
ENST00000584450.5:c.2532G>T	ENSP00000463714.1:p.Arg844Ser
ENST00000584601.5:c.2442G>T	ENSP00000462438.1:p.Arg814Ser
NM_001005862.2:c.2442G>T , LRG_724t1:c.2442G>T	NP_001005862.1:p.Arg814Ser
NM_001289936.1:c.2487G>T , LRG_724t4:c.2487G>T	NP_001276865.1:p.Arg829Ser
NM_001289937.1:c.2532G>T	NP_001276866.1:p.Arg844Ser
NM_004448.3:c.2532G>T , LRG_724t2:c.2532G>T	NP_004439.2:p.Arg844Ser
NR_110535.1:n.2856G>T
XM_024450641.1:c.2670G>T	XP_024306409.1:p.Arg890Ser
XM_024450642.1:c.2625G>T	XP_024306410.1:p.Arg875Ser
XM_024450643.1:c.2580G>T	XP_024306411.1:p.Arg860Ser
NM_001005862.3:c.2442G>T	NP_001005862.1:p.Arg814Ser
NM_001289936.2:c.2487G>T	NP_001276865.1:p.Arg829Ser
NM_001289937.2:c.2532G>T	NP_001276866.1:p.Arg844Ser
NM_001382782.1:c.2442G>T	NP_001369711.1:p.Arg814Ser
NM_001382783.1:c.2442G>T	NP_001369712.1:p.Arg814Ser
NM_001382784.1:c.2649G>T	NP_001369713.1:p.Arg883Ser
NM_001382785.1:c.2634G>T	NP_001369714.1:p.Arg878Ser
NM_001382786.1:c.2613G>T	NP_001369715.1:p.Arg871Ser
NM_001382787.1:c.2607G>T	NP_001369716.1:p.Arg869Ser
NM_001382788.1:c.2562G>T	NP_001369717.1:p.Arg854Ser
NM_001382789.1:c.2553G>T	NP_001369718.1:p.Arg851Ser
NM_001382790.1:c.2529G>T	NP_001369719.1:p.Arg843Ser
NM_001382791.1:c.2523G>T	NP_001369720.1:p.Arg841Ser
NM_001382792.1:c.2496G>T	NP_001369721.1:p.Arg832Ser
NM_001382793.1:c.2490G>T	NP_001369722.1:p.Arg830Ser
NM_001382794.1:c.2490G>T	NP_001369723.1:p.Arg830Ser
NM_001382795.1:c.2484G>T	NP_001369724.1:p.Arg828Ser
NM_001382796.1:c.2532G>T	NP_001369725.1:p.Arg844Ser
NM_001382797.1:c.2433G>T	NP_001369726.1:p.Arg811Ser
NM_001382798.1:c.2493+176G>T	NP_001369727.1:n.2493+176G>T
NM_001382799.1:c.2352G>T	NP_001369728.1:p.Arg784Ser
NM_001382800.1:c.2346G>T	NP_001369729.1:p.Arg782Ser
NM_001382801.1:c.2445+176G>T	NP_001369730.1:n.2445+176G>T
NM_001382802.1:c.2274G>T	NP_001369731.1:p.Arg758Ser
NM_001382803.1:c.2490G>T	NP_001369732.1:p.Arg830Ser
NM_001382804.1:c.1704G>T	NP_001369733.1:p.Arg568Ser
NM_001382805.1:c.2208+1427G>T	NP_001369734.1:n.2208+1427G>T
NM_001382806.1:c.1494G>T	NP_001369735.1:p.Arg498Ser
NM_004448.4:c.2532G>T MANE Select	NP_004439.2:p.Arg844Ser
NR_110535.2:n.2770G>T