Canonical Allele Identifier: CA399303443
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724844A>G , CM000679.2:g.39724844A>G GRCh38
NC_000017.10:g.37881097A>G , CM000679.1:g.37881097A>G GRCh37
NC_000017.9:g.35134623A>G NCBI36
NG_007503.1:g.41705A>G , LRG_724:g.41705A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2426A>G MANE Select ENSP00000269571.4:p.His809Arg
ENST00000269571.9:c.2426A>G ENSP00000269571.4:p.His809Arg
ENST00000406381.6:c.2336A>G ENSP00000385185.2:p.His779Arg
ENST00000445658.6:c.1598A>G ENSP00000404047.2:p.His533Arg
ENST00000541774.5:c.2381A>G ENSP00000446466.1:p.His794Arg
ENST00000578373.5:c.*2216A>G ENSP00000463427.1:n.*2216A>G
ENST00000580074.1:c.532A>G
ENST00000583038.5:n.3560A>G
ENST00000584450.5:c.2426A>G ENSP00000463714.1:p.His809Arg
ENST00000584601.5:c.2336A>G ENSP00000462438.1:p.His779Arg
NM_001005862.2:c.2336A>G , LRG_724t1:c.2336A>G NP_001005862.1:p.His779Arg
NM_001289936.1:c.2381A>G , LRG_724t4:c.2381A>G NP_001276865.1:p.His794Arg
NM_001289937.1:c.2426A>G NP_001276866.1:p.His809Arg
NM_004448.3:c.2426A>G , LRG_724t2:c.2426A>G NP_004439.2:p.His809Arg
NR_110535.1:n.2750A>G
XM_024450641.1:c.2564A>G XP_024306409.1:p.His855Arg
XM_024450642.1:c.2519A>G XP_024306410.1:p.His840Arg
XM_024450643.1:c.2474A>G XP_024306411.1:p.His825Arg
NM_001005862.3:c.2336A>G NP_001005862.1:p.His779Arg
NM_001289936.2:c.2381A>G NP_001276865.1:p.His794Arg
NM_001289937.2:c.2426A>G NP_001276866.1:p.His809Arg
NM_001382782.1:c.2336A>G NP_001369711.1:p.His779Arg
NM_001382783.1:c.2336A>G NP_001369712.1:p.His779Arg
NM_001382784.1:c.2543A>G NP_001369713.1:p.His848Arg
NM_001382785.1:c.2528A>G NP_001369714.1:p.His843Arg
NM_001382786.1:c.2507A>G NP_001369715.1:p.His836Arg
NM_001382787.1:c.2501A>G NP_001369716.1:p.His834Arg
NM_001382788.1:c.2456A>G NP_001369717.1:p.His819Arg
NM_001382789.1:c.2447A>G NP_001369718.1:p.His816Arg
NM_001382790.1:c.2423A>G NP_001369719.1:p.His808Arg
NM_001382791.1:c.2417A>G NP_001369720.1:p.His806Arg
NM_001382792.1:c.2390A>G NP_001369721.1:p.His797Arg
NM_001382793.1:c.2384A>G NP_001369722.1:p.His795Arg
NM_001382794.1:c.2384A>G NP_001369723.1:p.His795Arg
NM_001382795.1:c.2378A>G NP_001369724.1:p.His793Arg
NM_001382796.1:c.2426A>G NP_001369725.1:p.His809Arg
NM_001382797.1:c.2327A>G NP_001369726.1:p.His776Arg
NM_001382798.1:c.2426A>G NP_001369727.1:p.His809Arg
NM_001382799.1:c.2246A>G NP_001369728.1:p.His749Arg
NM_001382800.1:c.2308-205A>G NP_001369729.1:n.2308-205A>G
NM_001382801.1:c.2378A>G NP_001369730.1:p.His793Arg
NM_001382802.1:c.2168A>G NP_001369731.1:p.His723Arg
NM_001382803.1:c.2384A>G NP_001369732.1:p.His795Arg
NM_001382804.1:c.1598A>G NP_001369733.1:p.His533Arg
NM_001382805.1:c.2208+1184A>G NP_001369734.1:n.2208+1184A>G
NM_001382806.1:c.1388A>G NP_001369735.1:p.His463Arg
NM_004448.4:c.2426A>G MANE Select NP_004439.2:p.His809Arg
NR_110535.2:n.2664A>G