Canonical Allele Identifier: CA399292452
Community Standard Title: NM_004448.4(ERBB2):c.1556A>G (p.His519Arg)
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39716343A>G , CM000679.2:g.39716343A>G GRCh38
NC_000017.10:g.37872596A>G , CM000679.1:g.37872596A>G GRCh37
NC_000017.9:g.35126122A>G NCBI36
NG_007503.1:g.33204A>G , LRG_724:g.33204A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004448.4:c.1556A>G MANE Select NP_004439.2:p.His519Arg
ENST00000269571.10:c.1556A>G MANE Select ENSP00000269571.4:p.His519Arg
NM_001005862.2:c.1466A>G , LRG_724t1:c.1466A>G NP_001005862.1:p.His489Arg
NM_001005862.3:c.1466A>G NP_001005862.1:p.His489Arg
NM_001289936.1:c.1511A>G , LRG_724t4:c.1511A>G NP_001276865.1:p.His504Arg
NM_001289936.2:c.1511A>G NP_001276865.1:p.His504Arg
NM_001289937.1:c.1556A>G NP_001276866.1:p.His519Arg
NM_001289937.2:c.1556A>G NP_001276866.1:p.His519Arg
NM_001289938.1:c.1466A>G , LRG_724t3:c.1466A>G NP_001276867.1:p.His489Arg
NM_001289938.2:c.1466A>G NP_001276867.1:p.His489Arg
NM_001382782.1:c.1466A>G NP_001369711.1:p.His489Arg
NM_001382783.1:c.1466A>G NP_001369712.1:p.His489Arg
NM_001382784.1:c.1673A>G NP_001369713.1:p.His558Arg
NM_001382785.1:c.1556A>G NP_001369714.1:p.His519Arg
NM_001382786.1:c.1673A>G NP_001369715.1:p.His558Arg
NM_001382787.1:c.1631A>G NP_001369716.1:p.His544Arg
NM_001382788.1:c.1586A>G NP_001369717.1:p.His529Arg
NM_001382789.1:c.1577A>G NP_001369718.1:p.His526Arg
NM_001382790.1:c.1556A>G NP_001369719.1:p.His519Arg
NM_001382791.1:c.1547A>G NP_001369720.1:p.His516Arg
NM_001382792.1:c.1556A>G NP_001369721.1:p.His519Arg
NM_001382793.1:c.1556A>G NP_001369722.1:p.His519Arg
NM_001382794.1:c.1556A>G NP_001369723.1:p.His519Arg
NM_001382795.1:c.1556A>G NP_001369724.1:p.His519Arg
NM_001382796.1:c.1556A>G NP_001369725.1:p.His519Arg
NM_001382797.1:c.1556A>G NP_001369726.1:p.His519Arg
NM_001382798.1:c.1556A>G NP_001369727.1:p.His519Arg
NM_001382799.1:c.1376A>G NP_001369728.1:p.His459Arg
NM_001382800.1:c.1556A>G NP_001369729.1:p.His519Arg
NM_001382801.1:c.1556A>G NP_001369730.1:p.His519Arg
NM_001382802.1:c.1298A>G NP_001369731.1:p.His433Arg
NM_001382803.1:c.1556A>G NP_001369732.1:p.His519Arg
NM_001382804.1:c.728A>G NP_001369733.1:p.His243Arg
NM_001382805.1:c.1556A>G NP_001369734.1:p.His519Arg
NM_001382806.1:c.1222+984A>G NP_001369735.1:n.1222+984A>G
NM_004448.3:c.1556A>G , LRG_724t2:c.1556A>G NP_004439.2:p.His519Arg
NR_110535.1:n.1880A>G
NR_110535.2:n.1794A>G
ENST00000269571.9:c.1556A>G ENSP00000269571.4:p.His519Arg
ENST00000406381.6:c.1466A>G ENSP00000385185.2:p.His489Arg
ENST00000445658.6:c.728A>G ENSP00000404047.2:p.His243Arg
ENST00000541774.5:c.1511A>G ENSP00000446466.1:p.His504Arg
ENST00000578199.5:c.1466A>G ENSP00000462808.1:p.His489Arg
ENST00000578373.5:c.*1346A>G ENSP00000463427.1:n.*1346A>G
ENST00000582788.5:n.1406A>G
ENST00000583038.5:n.2609A>G
ENST00000584450.5:c.1556A>G ENSP00000463714.1:p.His519Arg
ENST00000584601.5:c.1466A>G ENSP00000462438.1:p.His489Arg
XM_024450641.1:c.1694A>G XP_024306409.1:p.His565Arg
XM_024450642.1:c.1649A>G XP_024306410.1:p.His550Arg
XM_024450643.1:c.1604A>G XP_024306411.1:p.His535Arg