Canonical Allele Identifier: CA399312533
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727464A>G , CM000679.2:g.39727464A>G GRCh38
NC_000017.10:g.37883717A>G , CM000679.1:g.37883717A>G GRCh37
NC_000017.9:g.35137243A>G NCBI36
NG_007503.1:g.44325A>G , LRG_724:g.44325A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3329A>G MANE Select ENSP00000269571.4:p.Gln1110Arg
ENST00000269571.9:c.3329A>G ENSP00000269571.4:p.Gln1110Arg
ENST00000406381.6:c.3239A>G ENSP00000385185.2:p.Gln1080Arg
ENST00000445658.6:c.2501A>G ENSP00000404047.2:p.Gln834Arg
ENST00000541774.5:c.3284A>G ENSP00000446466.1:p.Gln1095Arg
ENST00000578373.5:c.*3119A>G ENSP00000463427.1:n.*3119A>G
ENST00000584450.5:c.3160-225A>G ENSP00000463714.1:n.3160-225A>G
ENST00000584601.5:c.3239A>G ENSP00000462438.1:p.Gln1080Arg
NM_001005862.2:c.3239A>G , LRG_724t1:c.3239A>G NP_001005862.1:p.Gln1080Arg
NM_001289936.1:c.3284A>G , LRG_724t4:c.3284A>G NP_001276865.1:p.Gln1095Arg
NM_001289937.1:c.3160-225A>G NP_001276866.1:n.3160-225A>G
NM_004448.3:c.3329A>G , LRG_724t2:c.3329A>G NP_004439.2:p.Gln1110Arg
NR_110535.1:n.3653A>G
XM_024450641.1:c.3467A>G XP_024306409.1:p.Gln1156Arg
XM_024450642.1:c.3422A>G XP_024306410.1:p.Gln1141Arg
XM_024450643.1:c.3377A>G XP_024306411.1:p.Gln1126Arg
NM_001005862.3:c.3239A>G NP_001005862.1:p.Gln1080Arg
NM_001289936.2:c.3284A>G NP_001276865.1:p.Gln1095Arg
NM_001289937.2:c.3160-225A>G NP_001276866.1:n.3160-225A>G
NM_001382782.1:c.3239A>G NP_001369711.1:p.Gln1080Arg
NM_001382783.1:c.3239A>G NP_001369712.1:p.Gln1080Arg
NM_001382784.1:c.3446A>G NP_001369713.1:p.Gln1149Arg
NM_001382785.1:c.3431A>G NP_001369714.1:p.Gln1144Arg
NM_001382786.1:c.3410A>G NP_001369715.1:p.Gln1137Arg
NM_001382787.1:c.3404A>G NP_001369716.1:p.Gln1135Arg
NM_001382788.1:c.3359A>G NP_001369717.1:p.Gln1120Arg
NM_001382789.1:c.3350A>G NP_001369718.1:p.Gln1117Arg
NM_001382790.1:c.3326A>G NP_001369719.1:p.Gln1109Arg
NM_001382791.1:c.3320A>G NP_001369720.1:p.Gln1107Arg
NM_001382792.1:c.3293A>G NP_001369721.1:p.Gln1098Arg
NM_001382793.1:c.3287A>G NP_001369722.1:p.Gln1096Arg
NM_001382794.1:c.3287A>G NP_001369723.1:p.Gln1096Arg
NM_001382795.1:c.3281A>G NP_001369724.1:p.Gln1094Arg
NM_001382796.1:c.3242A>G NP_001369725.1:p.Gln1081Arg
NM_001382797.1:c.3230A>G NP_001369726.1:p.Gln1077Arg
NM_001382798.1:c.3173A>G NP_001369727.1:p.Gln1058Arg
NM_001382799.1:c.3149A>G NP_001369728.1:p.Gln1050Arg
NM_001382800.1:c.3143A>G NP_001369729.1:p.Gln1048Arg
NM_001382801.1:c.3125A>G NP_001369730.1:p.Gln1042Arg
NM_001382802.1:c.3071A>G NP_001369731.1:p.Gln1024Arg
NM_001382803.1:c.3118-225A>G NP_001369732.1:n.3118-225A>G
NM_001382804.1:c.2501A>G NP_001369733.1:p.Gln834Arg
NM_001382805.1:c.2378A>G NP_001369734.1:p.Gln793Arg
NM_001382806.1:c.2291A>G NP_001369735.1:p.Gln764Arg
NM_004448.4:c.3329A>G MANE Select NP_004439.2:p.Gln1110Arg
NR_110535.2:n.3567A>G