Canonical Allele Identifier: CA2259228119
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725056G= , CM000679.2:g.39725056G= GRCh38
NC_000017.10:g.37881309G= , CM000679.1:g.37881309G= GRCh37
NC_000017.9:g.35134835G= NCBI36
NG_007503.1:g.41917G= , LRG_724:g.41917G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2501G= MANE Select ENSP00000269571.4:p.Ser834=
ENST00000269571.9:c.2501G= ENSP00000269571.4:p.Ser834=
ENST00000406381.6:c.2411G= ENSP00000385185.2:p.Ser804=
ENST00000445658.6:c.1673G= ENSP00000404047.2:p.Ser558=
ENST00000541774.5:c.2456G= ENSP00000446466.1:p.Ser819=
ENST00000578373.5:c.*2291G= ENSP00000463427.1:n.*2291G=
ENST00000580074.1:c.607G=
ENST00000583038.5:n.3635G=
ENST00000584450.5:c.2501G= ENSP00000463714.1:p.Ser834=
ENST00000584601.5:c.2411G= ENSP00000462438.1:p.Ser804=
NM_001005862.2:c.2411G= , LRG_724t1:c.2411G= NP_001005862.1:p.Ser804=
NM_001289936.1:c.2456G= , LRG_724t4:c.2456G= NP_001276865.1:p.Ser819=
NM_001289937.1:c.2501G= NP_001276866.1:p.Ser834=
NM_004448.3:c.2501G= , LRG_724t2:c.2501G= NP_004439.2:p.Ser834=
NR_110535.1:n.2825G=
XM_024450641.1:c.2639G= XP_024306409.1:p.Ser880=
XM_024450642.1:c.2594G= XP_024306410.1:p.Ser865=
XM_024450643.1:c.2549G= XP_024306411.1:p.Ser850=
NM_001005862.3:c.2411G= NP_001005862.1:p.Ser804=
NM_001289936.2:c.2456G= NP_001276865.1:p.Ser819=
NM_001289937.2:c.2501G= NP_001276866.1:p.Ser834=
NM_001382782.1:c.2411G= NP_001369711.1:p.Ser804=
NM_001382783.1:c.2411G= NP_001369712.1:p.Ser804=
NM_001382784.1:c.2618G= NP_001369713.1:p.Ser873=
NM_001382785.1:c.2603G= NP_001369714.1:p.Ser868=
NM_001382786.1:c.2582G= NP_001369715.1:p.Ser861=
NM_001382787.1:c.2576G= NP_001369716.1:p.Ser859=
NM_001382788.1:c.2531G= NP_001369717.1:p.Ser844=
NM_001382789.1:c.2522G= NP_001369718.1:p.Ser841=
NM_001382790.1:c.2498G= NP_001369719.1:p.Ser833=
NM_001382791.1:c.2492G= NP_001369720.1:p.Ser831=
NM_001382792.1:c.2465G= NP_001369721.1:p.Ser822=
NM_001382793.1:c.2459G= NP_001369722.1:p.Ser820=
NM_001382794.1:c.2459G= NP_001369723.1:p.Ser820=
NM_001382795.1:c.2453G= NP_001369724.1:p.Ser818=
NM_001382796.1:c.2501G= NP_001369725.1:p.Ser834=
NM_001382797.1:c.2402G= NP_001369726.1:p.Ser801=
NM_001382798.1:c.2493+145G= NP_001369727.1:n.2493+145G=
NM_001382799.1:c.2321G= NP_001369728.1:p.Ser774=
NM_001382800.1:c.2315G= NP_001369729.1:p.Ser772=
NM_001382801.1:c.2445+145G= NP_001369730.1:n.2445+145G=
NM_001382802.1:c.2243G= NP_001369731.1:p.Ser748=
NM_001382803.1:c.2459G= NP_001369732.1:p.Ser820=
NM_001382804.1:c.1673G= NP_001369733.1:p.Ser558=
NM_001382805.1:c.2208+1396G= NP_001369734.1:n.2208+1396G=
NM_001382806.1:c.1463G= NP_001369735.1:p.Ser488=
NM_004448.4:c.2501G= MANE Select NP_004439.2:p.Ser834=
NR_110535.2:n.2739G=