Canonical Allele Identifier: CA2259228129
Gene: ERBB2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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