Canonical Allele Identifier: CA499890106

Gene: ERBB2

Linked Data

• dbSNP Id: rs1422047458
• gnomAD v2: 17-37881340-G-A
• gnomAD v4: 17-39725087-G-A
• MyVariant Identifiers: chr17:g.37881340G>A (hg19) ; chr17:g.39725087G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2532G>A MANE Select	ENSP00000269571.4:p.Arg844=
ENST00000269571.9:c.2532G>A	ENSP00000269571.4:p.Arg844=
ENST00000406381.6:c.2442G>A	ENSP00000385185.2:p.Arg814=
ENST00000445658.6:c.1704G>A	ENSP00000404047.2:p.Arg568=
ENST00000541774.5:c.2487G>A	ENSP00000446466.1:p.Arg829=
ENST00000578373.5:c.*2322G>A	ENSP00000463427.1:n.*2322G>A
ENST00000580074.1:c.638G>A
ENST00000583038.5:n.3666G>A
ENST00000584450.5:c.2532G>A	ENSP00000463714.1:p.Arg844=
ENST00000584601.5:c.2442G>A	ENSP00000462438.1:p.Arg814=
NM_001005862.2:c.2442G>A , LRG_724t1:c.2442G>A	NP_001005862.1:p.Arg814=
NM_001289936.1:c.2487G>A , LRG_724t4:c.2487G>A	NP_001276865.1:p.Arg829=
NM_001289937.1:c.2532G>A	NP_001276866.1:p.Arg844=
NM_004448.3:c.2532G>A , LRG_724t2:c.2532G>A	NP_004439.2:p.Arg844=
NR_110535.1:n.2856G>A
XM_024450641.1:c.2670G>A	XP_024306409.1:p.Arg890=
XM_024450642.1:c.2625G>A	XP_024306410.1:p.Arg875=
XM_024450643.1:c.2580G>A	XP_024306411.1:p.Arg860=
NM_001005862.3:c.2442G>A	NP_001005862.1:p.Arg814=
NM_001289936.2:c.2487G>A	NP_001276865.1:p.Arg829=
NM_001289937.2:c.2532G>A	NP_001276866.1:p.Arg844=
NM_001382782.1:c.2442G>A	NP_001369711.1:p.Arg814=
NM_001382783.1:c.2442G>A	NP_001369712.1:p.Arg814=
NM_001382784.1:c.2649G>A	NP_001369713.1:p.Arg883=
NM_001382785.1:c.2634G>A	NP_001369714.1:p.Arg878=
NM_001382786.1:c.2613G>A	NP_001369715.1:p.Arg871=
NM_001382787.1:c.2607G>A	NP_001369716.1:p.Arg869=
NM_001382788.1:c.2562G>A	NP_001369717.1:p.Arg854=
NM_001382789.1:c.2553G>A	NP_001369718.1:p.Arg851=
NM_001382790.1:c.2529G>A	NP_001369719.1:p.Arg843=
NM_001382791.1:c.2523G>A	NP_001369720.1:p.Arg841=
NM_001382792.1:c.2496G>A	NP_001369721.1:p.Arg832=
NM_001382793.1:c.2490G>A	NP_001369722.1:p.Arg830=
NM_001382794.1:c.2490G>A	NP_001369723.1:p.Arg830=
NM_001382795.1:c.2484G>A	NP_001369724.1:p.Arg828=
NM_001382796.1:c.2532G>A	NP_001369725.1:p.Arg844=
NM_001382797.1:c.2433G>A	NP_001369726.1:p.Arg811=
NM_001382798.1:c.2493+176G>A	NP_001369727.1:n.2493+176G>A
NM_001382799.1:c.2352G>A	NP_001369728.1:p.Arg784=
NM_001382800.1:c.2346G>A	NP_001369729.1:p.Arg782=
NM_001382801.1:c.2445+176G>A	NP_001369730.1:n.2445+176G>A
NM_001382802.1:c.2274G>A	NP_001369731.1:p.Arg758=
NM_001382803.1:c.2490G>A	NP_001369732.1:p.Arg830=
NM_001382804.1:c.1704G>A	NP_001369733.1:p.Arg568=
NM_001382805.1:c.2208+1427G>A	NP_001369734.1:n.2208+1427G>A
NM_001382806.1:c.1494G>A	NP_001369735.1:p.Arg498=
NM_004448.4:c.2532G>A MANE Select	NP_004439.2:p.Arg844=
NR_110535.2:n.2770G>A