Canonical Allele Identifier: CA2259228141
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725118A= , CM000679.2:g.39725118A= GRCh38
NC_000017.10:g.37881371A= , CM000679.1:g.37881371A= GRCh37
NC_000017.9:g.35134897A= NCBI36
NG_007503.1:g.41979A= , LRG_724:g.41979A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2563A= MANE Select ENSP00000269571.4:p.Ser855=
ENST00000269571.9:c.2563A= ENSP00000269571.4:p.Ser855=
ENST00000406381.6:c.2473A= ENSP00000385185.2:p.Ser825=
ENST00000445658.6:c.1735A= ENSP00000404047.2:p.Ser579=
ENST00000541774.5:c.2518A= ENSP00000446466.1:p.Ser840=
ENST00000578373.5:c.*2353A= ENSP00000463427.1:n.*2353A=
ENST00000580074.1:c.669A=
ENST00000583038.5:n.3697A=
ENST00000584450.5:c.2563A= ENSP00000463714.1:p.Ser855=
ENST00000584601.5:c.2473A= ENSP00000462438.1:p.Ser825=
NM_001005862.2:c.2473A= , LRG_724t1:c.2473A= NP_001005862.1:p.Ser825=
NM_001289936.1:c.2518A= , LRG_724t4:c.2518A= NP_001276865.1:p.Ser840=
NM_001289937.1:c.2563A= NP_001276866.1:p.Ser855=
NM_004448.3:c.2563A= , LRG_724t2:c.2563A= NP_004439.2:p.Ser855=
NR_110535.1:n.2887A=
XM_024450641.1:c.2701A= XP_024306409.1:p.Ser901=
XM_024450642.1:c.2656A= XP_024306410.1:p.Ser886=
XM_024450643.1:c.2611A= XP_024306411.1:p.Ser871=
NM_001005862.3:c.2473A= NP_001005862.1:p.Ser825=
NM_001289936.2:c.2518A= NP_001276865.1:p.Ser840=
NM_001289937.2:c.2563A= NP_001276866.1:p.Ser855=
NM_001382782.1:c.2473A= NP_001369711.1:p.Ser825=
NM_001382783.1:c.2473A= NP_001369712.1:p.Ser825=
NM_001382784.1:c.2680A= NP_001369713.1:p.Ser894=
NM_001382785.1:c.2665A= NP_001369714.1:p.Ser889=
NM_001382786.1:c.2644A= NP_001369715.1:p.Ser882=
NM_001382787.1:c.2638A= NP_001369716.1:p.Ser880=
NM_001382788.1:c.2593A= NP_001369717.1:p.Ser865=
NM_001382789.1:c.2584A= NP_001369718.1:p.Ser862=
NM_001382790.1:c.2560A= NP_001369719.1:p.Ser854=
NM_001382791.1:c.2554A= NP_001369720.1:p.Ser852=
NM_001382792.1:c.2527A= NP_001369721.1:p.Ser843=
NM_001382793.1:c.2521A= NP_001369722.1:p.Ser841=
NM_001382794.1:c.2521A= NP_001369723.1:p.Ser841=
NM_001382795.1:c.2515A= NP_001369724.1:p.Ser839=
NM_001382796.1:c.2563A= NP_001369725.1:p.Ser855=
NM_001382797.1:c.2464A= NP_001369726.1:p.Ser822=
NM_001382798.1:c.2493+207A= NP_001369727.1:n.2493+207A=
NM_001382799.1:c.2383A= NP_001369728.1:p.Ser795=
NM_001382800.1:c.2377A= NP_001369729.1:p.Ser793=
NM_001382801.1:c.2445+207A= NP_001369730.1:n.2445+207A=
NM_001382802.1:c.2305A= NP_001369731.1:p.Ser769=
NM_001382803.1:c.2521A= NP_001369732.1:p.Ser841=
NM_001382804.1:c.1735A= NP_001369733.1:p.Ser579=
NM_001382805.1:c.2208+1458A= NP_001369734.1:n.2208+1458A=
NM_001382806.1:c.1525A= NP_001369735.1:p.Ser509=
NM_004448.4:c.2563A= MANE Select NP_004439.2:p.Ser855=
NR_110535.2:n.2801A=