Canonical Allele Identifier: CA2259228142
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725123C= , CM000679.2:g.39725123C= GRCh38
NC_000017.10:g.37881376C= , CM000679.1:g.37881376C= GRCh37
NC_000017.9:g.35134902C= NCBI36
NG_007503.1:g.41984C= , LRG_724:g.41984C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2568C= MANE Select ENSP00000269571.4:p.Pro856=
ENST00000269571.9:c.2568C= ENSP00000269571.4:p.Pro856=
ENST00000406381.6:c.2478C= ENSP00000385185.2:p.Pro826=
ENST00000445658.6:c.1740C= ENSP00000404047.2:p.Pro580=
ENST00000541774.5:c.2523C= ENSP00000446466.1:p.Pro841=
ENST00000578373.5:c.*2358C= ENSP00000463427.1:n.*2358C=
ENST00000580074.1:c.674C=
ENST00000583038.5:n.3702C=
ENST00000584450.5:c.2568C= ENSP00000463714.1:p.Pro856=
ENST00000584601.5:c.2478C= ENSP00000462438.1:p.Pro826=
NM_001005862.2:c.2478C= , LRG_724t1:c.2478C= NP_001005862.1:p.Pro826=
NM_001289936.1:c.2523C= , LRG_724t4:c.2523C= NP_001276865.1:p.Pro841=
NM_001289937.1:c.2568C= NP_001276866.1:p.Pro856=
NM_004448.3:c.2568C= , LRG_724t2:c.2568C= NP_004439.2:p.Pro856=
NR_110535.1:n.2892C=
XM_024450641.1:c.2706C= XP_024306409.1:p.Pro902=
XM_024450642.1:c.2661C= XP_024306410.1:p.Pro887=
XM_024450643.1:c.2616C= XP_024306411.1:p.Pro872=
NM_001005862.3:c.2478C= NP_001005862.1:p.Pro826=
NM_001289936.2:c.2523C= NP_001276865.1:p.Pro841=
NM_001289937.2:c.2568C= NP_001276866.1:p.Pro856=
NM_001382782.1:c.2478C= NP_001369711.1:p.Pro826=
NM_001382783.1:c.2478C= NP_001369712.1:p.Pro826=
NM_001382784.1:c.2685C= NP_001369713.1:p.Pro895=
NM_001382785.1:c.2670C= NP_001369714.1:p.Pro890=
NM_001382786.1:c.2649C= NP_001369715.1:p.Pro883=
NM_001382787.1:c.2643C= NP_001369716.1:p.Pro881=
NM_001382788.1:c.2598C= NP_001369717.1:p.Pro866=
NM_001382789.1:c.2589C= NP_001369718.1:p.Pro863=
NM_001382790.1:c.2565C= NP_001369719.1:p.Pro855=
NM_001382791.1:c.2559C= NP_001369720.1:p.Pro853=
NM_001382792.1:c.2532C= NP_001369721.1:p.Pro844=
NM_001382793.1:c.2526C= NP_001369722.1:p.Pro842=
NM_001382794.1:c.2526C= NP_001369723.1:p.Pro842=
NM_001382795.1:c.2520C= NP_001369724.1:p.Pro840=
NM_001382796.1:c.2568C= NP_001369725.1:p.Pro856=
NM_001382797.1:c.2469C= NP_001369726.1:p.Pro823=
NM_001382798.1:c.2494-204C= NP_001369727.1:n.2494-204C=
NM_001382799.1:c.2388C= NP_001369728.1:p.Pro796=
NM_001382800.1:c.2382C= NP_001369729.1:p.Pro794=
NM_001382801.1:c.2446-204C= NP_001369730.1:n.2446-204C=
NM_001382802.1:c.2310C= NP_001369731.1:p.Pro770=
NM_001382803.1:c.2526C= NP_001369732.1:p.Pro842=
NM_001382804.1:c.1740C= NP_001369733.1:p.Pro580=
NM_001382805.1:c.2208+1463C= NP_001369734.1:n.2208+1463C=
NM_001382806.1:c.1530C= NP_001369735.1:p.Pro510=
NM_004448.4:c.2568C= MANE Select NP_004439.2:p.Pro856=
NR_110535.2:n.2806C=