Canonical Allele Identifier: CA399310374
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727359T>G , CM000679.2:g.39727359T>G GRCh38
NC_000017.10:g.37883612T>G , CM000679.1:g.37883612T>G GRCh37
NC_000017.9:g.35137138T>G NCBI36
NG_007503.1:g.44220T>G , LRG_724:g.44220T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3224T>G MANE Select ENSP00000269571.4:p.Leu1075Arg
ENST00000269571.9:c.3224T>G ENSP00000269571.4:p.Leu1075Arg
ENST00000406381.6:c.3134T>G ENSP00000385185.2:p.Leu1045Arg
ENST00000445658.6:c.2396T>G ENSP00000404047.2:p.Leu799Arg
ENST00000541774.5:c.3179T>G ENSP00000446466.1:p.Leu1060Arg
ENST00000578373.5:c.*3014T>G ENSP00000463427.1:n.*3014T>G
ENST00000584450.5:c.3160-330T>G ENSP00000463714.1:n.3160-330T>G
ENST00000584601.5:c.3134T>G ENSP00000462438.1:p.Leu1045Arg
NM_001005862.2:c.3134T>G , LRG_724t1:c.3134T>G NP_001005862.1:p.Leu1045Arg
NM_001289936.1:c.3179T>G , LRG_724t4:c.3179T>G NP_001276865.1:p.Leu1060Arg
NM_001289937.1:c.3160-330T>G NP_001276866.1:n.3160-330T>G
NM_004448.3:c.3224T>G , LRG_724t2:c.3224T>G NP_004439.2:p.Leu1075Arg
NR_110535.1:n.3548T>G
XM_024450641.1:c.3362T>G XP_024306409.1:p.Leu1121Arg
XM_024450642.1:c.3317T>G XP_024306410.1:p.Leu1106Arg
XM_024450643.1:c.3272T>G XP_024306411.1:p.Leu1091Arg
NM_001005862.3:c.3134T>G NP_001005862.1:p.Leu1045Arg
NM_001289936.2:c.3179T>G NP_001276865.1:p.Leu1060Arg
NM_001289937.2:c.3160-330T>G NP_001276866.1:n.3160-330T>G
NM_001382782.1:c.3134T>G NP_001369711.1:p.Leu1045Arg
NM_001382783.1:c.3134T>G NP_001369712.1:p.Leu1045Arg
NM_001382784.1:c.3341T>G NP_001369713.1:p.Leu1114Arg
NM_001382785.1:c.3326T>G NP_001369714.1:p.Leu1109Arg
NM_001382786.1:c.3305T>G NP_001369715.1:p.Leu1102Arg
NM_001382787.1:c.3299T>G NP_001369716.1:p.Leu1100Arg
NM_001382788.1:c.3254T>G NP_001369717.1:p.Leu1085Arg
NM_001382789.1:c.3245T>G NP_001369718.1:p.Leu1082Arg
NM_001382790.1:c.3221T>G NP_001369719.1:p.Leu1074Arg
NM_001382791.1:c.3215T>G NP_001369720.1:p.Leu1072Arg
NM_001382792.1:c.3188T>G NP_001369721.1:p.Leu1063Arg
NM_001382793.1:c.3182T>G NP_001369722.1:p.Leu1061Arg
NM_001382794.1:c.3182T>G NP_001369723.1:p.Leu1061Arg
NM_001382795.1:c.3176T>G NP_001369724.1:p.Leu1059Arg
NM_001382796.1:c.3137T>G NP_001369725.1:p.Leu1046Arg
NM_001382797.1:c.3125T>G NP_001369726.1:p.Leu1042Arg
NM_001382798.1:c.3068T>G NP_001369727.1:p.Leu1023Arg
NM_001382799.1:c.3044T>G NP_001369728.1:p.Leu1015Arg
NM_001382800.1:c.3038T>G NP_001369729.1:p.Leu1013Arg
NM_001382801.1:c.3020T>G NP_001369730.1:p.Leu1007Arg
NM_001382802.1:c.2966T>G NP_001369731.1:p.Leu989Arg
NM_001382803.1:c.3118-330T>G NP_001369732.1:n.3118-330T>G
NM_001382804.1:c.2396T>G NP_001369733.1:p.Leu799Arg
NM_001382805.1:c.2273T>G NP_001369734.1:p.Leu758Arg
NM_001382806.1:c.2186T>G NP_001369735.1:p.Leu729Arg
NM_004448.4:c.3224T>G MANE Select NP_004439.2:p.Leu1075Arg
NR_110535.2:n.3462T>G