Canonical Allele Identifier: CA2259227604
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724010C= , CM000679.2:g.39724010C= GRCh38
NC_000017.10:g.37880263C= , CM000679.1:g.37880263C= GRCh37
NC_000017.9:g.35133789C= NCBI36
NG_007503.1:g.40871C= , LRG_724:g.40871C=

Transcript Alleles

HGVS Amino-acid change
ENST00000269571.10:c.2307C= MANE Select ENSP00000269571.4:p.Asp769=
ENST00000269571.9:c.2307C= ENSP00000269571.4:p.Asp769=
ENST00000406381.6:c.2217C= ENSP00000385185.2:p.Asp739=
ENST00000445658.6:c.1479C= ENSP00000404047.2:p.Asp493=
ENST00000541774.5:c.2262C= ENSP00000446466.1:p.Asp754=
ENST00000578373.5:c.*2097C= ENSP00000463427.1:n.*2097C=
ENST00000580074.1:c.413C=
ENST00000583038.5:n.3441C=
ENST00000584450.5:c.2307C= ENSP00000463714.1:p.Asp769=
ENST00000584601.5:c.2217C= ENSP00000462438.1:p.Asp739=
NM_001005862.2:c.2217C= , LRG_724t1:c.2217C= NP_001005862.1:p.Asp739=
NM_001289936.1:c.2262C= , LRG_724t4:c.2262C= NP_001276865.1:p.Asp754=
NM_001289937.1:c.2307C= NP_001276866.1:p.Asp769=
NM_004448.3:c.2307C= , LRG_724t2:c.2307C= NP_004439.2:p.Asp769=
NR_110535.1:n.2631C=
XM_024450641.1:c.2445C= XP_024306409.1:p.Asp815=
XM_024450642.1:c.2400C= XP_024306410.1:p.Asp800=
XM_024450643.1:c.2355C= XP_024306411.1:p.Asp785=
NM_001005862.3:c.2217C= NP_001005862.1:p.Asp739=
NM_001289936.2:c.2262C= NP_001276865.1:p.Asp754=
NM_001289937.2:c.2307C= NP_001276866.1:p.Asp769=
NM_001382782.1:c.2217C= NP_001369711.1:p.Asp739=
NM_001382783.1:c.2217C= NP_001369712.1:p.Asp739=
NM_001382784.1:c.2424C= NP_001369713.1:p.Asp808=
NM_001382785.1:c.2409C= NP_001369714.1:p.Asp803=
NM_001382786.1:c.2388C= NP_001369715.1:p.Asp796=
NM_001382787.1:c.2382C= NP_001369716.1:p.Asp794=
NM_001382788.1:c.2337C= NP_001369717.1:p.Asp779=
NM_001382789.1:c.2328C= NP_001369718.1:p.Asp776=
NM_001382790.1:c.2304C= NP_001369719.1:p.Asp768=
NM_001382791.1:c.2298C= NP_001369720.1:p.Asp766=
NM_001382792.1:c.2271C= NP_001369721.1:p.Asp757=
NM_001382793.1:c.2265C= NP_001369722.1:p.Asp755=
NM_001382794.1:c.2265C= NP_001369723.1:p.Asp755=
NM_001382795.1:c.2259C= NP_001369724.1:p.Asp753=
NM_001382796.1:c.2307C= NP_001369725.1:p.Asp769=
NM_001382797.1:c.2208+350C= NP_001369726.1:n.2208+350C=
NM_001382798.1:c.2307C= NP_001369727.1:p.Asp769=
NM_001382799.1:c.2127C= NP_001369728.1:p.Asp709=
NM_001382800.1:c.2307C= NP_001369729.1:p.Asp769=
NM_001382801.1:c.2259C= NP_001369730.1:p.Asp753=
NM_001382802.1:c.2049C= NP_001369731.1:p.Asp683=
NM_001382803.1:c.2265C= NP_001369732.1:p.Asp755=
NM_001382804.1:c.1479C= NP_001369733.1:p.Asp493=
NM_001382805.1:c.2208+350C= NP_001369734.1:n.2208+350C=
NM_001382806.1:c.1269C= NP_001369735.1:p.Asp423=
NM_004448.4:c.2307C= MANE Select NP_004439.2:p.Asp769=
NR_110535.2:n.2545C=