Canonical Allele Identifier: CA399303352
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145851232

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724831T>A , CM000679.2:g.39724831T>A GRCh38
NC_000017.10:g.37881084T>A , CM000679.1:g.37881084T>A GRCh37
NC_000017.9:g.35134610T>A NCBI36
NG_007503.1:g.41692T>A , LRG_724:g.41692T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2413T>A MANE Select ENSP00000269571.4:p.Cys805Ser
ENST00000269571.9:c.2413T>A ENSP00000269571.4:p.Cys805Ser
ENST00000406381.6:c.2323T>A ENSP00000385185.2:p.Cys775Ser
ENST00000445658.6:c.1585T>A ENSP00000404047.2:p.Cys529Ser
ENST00000541774.5:c.2368T>A ENSP00000446466.1:p.Cys790Ser
ENST00000578373.5:c.*2203T>A ENSP00000463427.1:n.*2203T>A
ENST00000580074.1:c.519T>A
ENST00000583038.5:n.3547T>A
ENST00000584450.5:c.2413T>A ENSP00000463714.1:p.Cys805Ser
ENST00000584601.5:c.2323T>A ENSP00000462438.1:p.Cys775Ser
NM_001005862.2:c.2323T>A , LRG_724t1:c.2323T>A NP_001005862.1:p.Cys775Ser
NM_001289936.1:c.2368T>A , LRG_724t4:c.2368T>A NP_001276865.1:p.Cys790Ser
NM_001289937.1:c.2413T>A NP_001276866.1:p.Cys805Ser
NM_004448.3:c.2413T>A , LRG_724t2:c.2413T>A NP_004439.2:p.Cys805Ser
NR_110535.1:n.2737T>A
XM_024450641.1:c.2551T>A XP_024306409.1:p.Cys851Ser
XM_024450642.1:c.2506T>A XP_024306410.1:p.Cys836Ser
XM_024450643.1:c.2461T>A XP_024306411.1:p.Cys821Ser
NM_001005862.3:c.2323T>A NP_001005862.1:p.Cys775Ser
NM_001289936.2:c.2368T>A NP_001276865.1:p.Cys790Ser
NM_001289937.2:c.2413T>A NP_001276866.1:p.Cys805Ser
NM_001382782.1:c.2323T>A NP_001369711.1:p.Cys775Ser
NM_001382783.1:c.2323T>A NP_001369712.1:p.Cys775Ser
NM_001382784.1:c.2530T>A NP_001369713.1:p.Cys844Ser
NM_001382785.1:c.2515T>A NP_001369714.1:p.Cys839Ser
NM_001382786.1:c.2494T>A NP_001369715.1:p.Cys832Ser
NM_001382787.1:c.2488T>A NP_001369716.1:p.Cys830Ser
NM_001382788.1:c.2443T>A NP_001369717.1:p.Cys815Ser
NM_001382789.1:c.2434T>A NP_001369718.1:p.Cys812Ser
NM_001382790.1:c.2410T>A NP_001369719.1:p.Cys804Ser
NM_001382791.1:c.2404T>A NP_001369720.1:p.Cys802Ser
NM_001382792.1:c.2377T>A NP_001369721.1:p.Cys793Ser
NM_001382793.1:c.2371T>A NP_001369722.1:p.Cys791Ser
NM_001382794.1:c.2371T>A NP_001369723.1:p.Cys791Ser
NM_001382795.1:c.2365T>A NP_001369724.1:p.Cys789Ser
NM_001382796.1:c.2413T>A NP_001369725.1:p.Cys805Ser
NM_001382797.1:c.2314T>A NP_001369726.1:p.Cys772Ser
NM_001382798.1:c.2413T>A NP_001369727.1:p.Cys805Ser
NM_001382799.1:c.2233T>A NP_001369728.1:p.Cys745Ser
NM_001382800.1:c.2308-218T>A NP_001369729.1:n.2308-218T>A
NM_001382801.1:c.2365T>A NP_001369730.1:p.Cys789Ser
NM_001382802.1:c.2155T>A NP_001369731.1:p.Cys719Ser
NM_001382803.1:c.2371T>A NP_001369732.1:p.Cys791Ser
NM_001382804.1:c.1585T>A NP_001369733.1:p.Cys529Ser
NM_001382805.1:c.2208+1171T>A NP_001369734.1:n.2208+1171T>A
NM_001382806.1:c.1375T>A NP_001369735.1:p.Cys459Ser
NM_004448.4:c.2413T>A MANE Select NP_004439.2:p.Cys805Ser
NR_110535.2:n.2651T>A