Canonical Allele Identifier: CA399312674
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727499T>C , CM000679.2:g.39727499T>C GRCh38
NC_000017.10:g.37883752T>C , CM000679.1:g.37883752T>C GRCh37
NC_000017.9:g.35137278T>C NCBI36
NG_007503.1:g.44360T>C , LRG_724:g.44360T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3364T>C MANE Select ENSP00000269571.4:p.Ser1122Pro
ENST00000269571.9:c.3364T>C ENSP00000269571.4:p.Ser1122Pro
ENST00000406381.6:c.3274T>C ENSP00000385185.2:p.Ser1092Pro
ENST00000445658.6:c.2536T>C ENSP00000404047.2:p.Ser846Pro
ENST00000541774.5:c.3319T>C ENSP00000446466.1:p.Ser1107Pro
ENST00000578373.5:c.*3154T>C ENSP00000463427.1:n.*3154T>C
ENST00000584450.5:c.3160-190T>C ENSP00000463714.1:n.3160-190T>C
ENST00000584601.5:c.3274T>C ENSP00000462438.1:p.Ser1092Pro
NM_001005862.2:c.3274T>C , LRG_724t1:c.3274T>C NP_001005862.1:p.Ser1092Pro
NM_001289936.1:c.3319T>C , LRG_724t4:c.3319T>C NP_001276865.1:p.Ser1107Pro
NM_001289937.1:c.3160-190T>C NP_001276866.1:n.3160-190T>C
NM_004448.3:c.3364T>C , LRG_724t2:c.3364T>C NP_004439.2:p.Ser1122Pro
NR_110535.1:n.3688T>C
XM_024450641.1:c.3502T>C XP_024306409.1:p.Ser1168Pro
XM_024450642.1:c.3457T>C XP_024306410.1:p.Ser1153Pro
XM_024450643.1:c.3412T>C XP_024306411.1:p.Ser1138Pro
NM_001005862.3:c.3274T>C NP_001005862.1:p.Ser1092Pro
NM_001289936.2:c.3319T>C NP_001276865.1:p.Ser1107Pro
NM_001289937.2:c.3160-190T>C NP_001276866.1:n.3160-190T>C
NM_001382782.1:c.3274T>C NP_001369711.1:p.Ser1092Pro
NM_001382783.1:c.3274T>C NP_001369712.1:p.Ser1092Pro
NM_001382784.1:c.3481T>C NP_001369713.1:p.Ser1161Pro
NM_001382785.1:c.3466T>C NP_001369714.1:p.Ser1156Pro
NM_001382786.1:c.3445T>C NP_001369715.1:p.Ser1149Pro
NM_001382787.1:c.3439T>C NP_001369716.1:p.Ser1147Pro
NM_001382788.1:c.3394T>C NP_001369717.1:p.Ser1132Pro
NM_001382789.1:c.3385T>C NP_001369718.1:p.Ser1129Pro
NM_001382790.1:c.3361T>C NP_001369719.1:p.Ser1121Pro
NM_001382791.1:c.3355T>C NP_001369720.1:p.Ser1119Pro
NM_001382792.1:c.3328T>C NP_001369721.1:p.Ser1110Pro
NM_001382793.1:c.3322T>C NP_001369722.1:p.Ser1108Pro
NM_001382794.1:c.3322T>C NP_001369723.1:p.Ser1108Pro
NM_001382795.1:c.3316T>C NP_001369724.1:p.Ser1106Pro
NM_001382796.1:c.3277T>C NP_001369725.1:p.Ser1093Pro
NM_001382797.1:c.3265T>C NP_001369726.1:p.Ser1089Pro
NM_001382798.1:c.3208T>C NP_001369727.1:p.Ser1070Pro
NM_001382799.1:c.3184T>C NP_001369728.1:p.Ser1062Pro
NM_001382800.1:c.3178T>C NP_001369729.1:p.Ser1060Pro
NM_001382801.1:c.3160T>C NP_001369730.1:p.Ser1054Pro
NM_001382802.1:c.3106T>C NP_001369731.1:p.Ser1036Pro
NM_001382803.1:c.3118-190T>C NP_001369732.1:n.3118-190T>C
NM_001382804.1:c.2536T>C NP_001369733.1:p.Ser846Pro
NM_001382805.1:c.2413T>C NP_001369734.1:p.Ser805Pro
NM_001382806.1:c.2326T>C NP_001369735.1:p.Ser776Pro
NM_004448.4:c.3364T>C MANE Select NP_004439.2:p.Ser1122Pro
NR_110535.2:n.3602T>C