Canonical Allele Identifier: CA399312673

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143255239
• MyVariant Identifiers: chr17:g.37883752T>A (hg19) ; chr17:g.39727499T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3364T>A MANE Select	ENSP00000269571.4:p.Ser1122Thr
ENST00000269571.9:c.3364T>A	ENSP00000269571.4:p.Ser1122Thr
ENST00000406381.6:c.3274T>A	ENSP00000385185.2:p.Ser1092Thr
ENST00000445658.6:c.2536T>A	ENSP00000404047.2:p.Ser846Thr
ENST00000541774.5:c.3319T>A	ENSP00000446466.1:p.Ser1107Thr
ENST00000578373.5:c.*3154T>A	ENSP00000463427.1:n.*3154T>A
ENST00000584450.5:c.3160-190T>A	ENSP00000463714.1:n.3160-190T>A
ENST00000584601.5:c.3274T>A	ENSP00000462438.1:p.Ser1092Thr
NM_001005862.2:c.3274T>A , LRG_724t1:c.3274T>A	NP_001005862.1:p.Ser1092Thr
NM_001289936.1:c.3319T>A , LRG_724t4:c.3319T>A	NP_001276865.1:p.Ser1107Thr
NM_001289937.1:c.3160-190T>A	NP_001276866.1:n.3160-190T>A
NM_004448.3:c.3364T>A , LRG_724t2:c.3364T>A	NP_004439.2:p.Ser1122Thr
NR_110535.1:n.3688T>A
XM_024450641.1:c.3502T>A	XP_024306409.1:p.Ser1168Thr
XM_024450642.1:c.3457T>A	XP_024306410.1:p.Ser1153Thr
XM_024450643.1:c.3412T>A	XP_024306411.1:p.Ser1138Thr
NM_001005862.3:c.3274T>A	NP_001005862.1:p.Ser1092Thr
NM_001289936.2:c.3319T>A	NP_001276865.1:p.Ser1107Thr
NM_001289937.2:c.3160-190T>A	NP_001276866.1:n.3160-190T>A
NM_001382782.1:c.3274T>A	NP_001369711.1:p.Ser1092Thr
NM_001382783.1:c.3274T>A	NP_001369712.1:p.Ser1092Thr
NM_001382784.1:c.3481T>A	NP_001369713.1:p.Ser1161Thr
NM_001382785.1:c.3466T>A	NP_001369714.1:p.Ser1156Thr
NM_001382786.1:c.3445T>A	NP_001369715.1:p.Ser1149Thr
NM_001382787.1:c.3439T>A	NP_001369716.1:p.Ser1147Thr
NM_001382788.1:c.3394T>A	NP_001369717.1:p.Ser1132Thr
NM_001382789.1:c.3385T>A	NP_001369718.1:p.Ser1129Thr
NM_001382790.1:c.3361T>A	NP_001369719.1:p.Ser1121Thr
NM_001382791.1:c.3355T>A	NP_001369720.1:p.Ser1119Thr
NM_001382792.1:c.3328T>A	NP_001369721.1:p.Ser1110Thr
NM_001382793.1:c.3322T>A	NP_001369722.1:p.Ser1108Thr
NM_001382794.1:c.3322T>A	NP_001369723.1:p.Ser1108Thr
NM_001382795.1:c.3316T>A	NP_001369724.1:p.Ser1106Thr
NM_001382796.1:c.3277T>A	NP_001369725.1:p.Ser1093Thr
NM_001382797.1:c.3265T>A	NP_001369726.1:p.Ser1089Thr
NM_001382798.1:c.3208T>A	NP_001369727.1:p.Ser1070Thr
NM_001382799.1:c.3184T>A	NP_001369728.1:p.Ser1062Thr
NM_001382800.1:c.3178T>A	NP_001369729.1:p.Ser1060Thr
NM_001382801.1:c.3160T>A	NP_001369730.1:p.Ser1054Thr
NM_001382802.1:c.3106T>A	NP_001369731.1:p.Ser1036Thr
NM_001382803.1:c.3118-190T>A	NP_001369732.1:n.3118-190T>A
NM_001382804.1:c.2536T>A	NP_001369733.1:p.Ser846Thr
NM_001382805.1:c.2413T>A	NP_001369734.1:p.Ser805Thr
NM_001382806.1:c.2326T>A	NP_001369735.1:p.Ser776Thr
NM_004448.4:c.3364T>A MANE Select	NP_004439.2:p.Ser1122Thr
NR_110535.2:n.3602T>A