Canonical Allele Identifier: CA399310225

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143235532
• MyVariant Identifiers: chr17:g.37883584T>A (hg19) ; chr17:g.39727331T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727331T>A , CM000679.2:g.39727331T>A	GRCh38
NC_000017.10:g.37883584T>A , CM000679.1:g.37883584T>A	GRCh37
NC_000017.9:g.35137110T>A	NCBI36
NG_007503.1:g.44192T>A , LRG_724:g.44192T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3196T>A MANE Select	ENSP00000269571.4:p.Ser1066Thr
ENST00000269571.9:c.3196T>A	ENSP00000269571.4:p.Ser1066Thr
ENST00000406381.6:c.3106T>A	ENSP00000385185.2:p.Ser1036Thr
ENST00000445658.6:c.2368T>A	ENSP00000404047.2:p.Ser790Thr
ENST00000541774.5:c.3151T>A	ENSP00000446466.1:p.Ser1051Thr
ENST00000578373.5:c.*2986T>A	ENSP00000463427.1:n.*2986T>A
ENST00000584450.5:c.3159+328T>A	ENSP00000463714.1:n.3159+328T>A
ENST00000584601.5:c.3106T>A	ENSP00000462438.1:p.Ser1036Thr
NM_001005862.2:c.3106T>A , LRG_724t1:c.3106T>A	NP_001005862.1:p.Ser1036Thr
NM_001289936.1:c.3151T>A , LRG_724t4:c.3151T>A	NP_001276865.1:p.Ser1051Thr
NM_001289937.1:c.3159+328T>A	NP_001276866.1:n.3159+328T>A
NM_004448.3:c.3196T>A , LRG_724t2:c.3196T>A	NP_004439.2:p.Ser1066Thr
NR_110535.1:n.3520T>A
XM_024450641.1:c.3334T>A	XP_024306409.1:p.Ser1112Thr
XM_024450642.1:c.3289T>A	XP_024306410.1:p.Ser1097Thr
XM_024450643.1:c.3244T>A	XP_024306411.1:p.Ser1082Thr
NM_001005862.3:c.3106T>A	NP_001005862.1:p.Ser1036Thr
NM_001289936.2:c.3151T>A	NP_001276865.1:p.Ser1051Thr
NM_001289937.2:c.3159+328T>A	NP_001276866.1:n.3159+328T>A
NM_001382782.1:c.3106T>A	NP_001369711.1:p.Ser1036Thr
NM_001382783.1:c.3106T>A	NP_001369712.1:p.Ser1036Thr
NM_001382784.1:c.3313T>A	NP_001369713.1:p.Ser1105Thr
NM_001382785.1:c.3298T>A	NP_001369714.1:p.Ser1100Thr
NM_001382786.1:c.3277T>A	NP_001369715.1:p.Ser1093Thr
NM_001382787.1:c.3271T>A	NP_001369716.1:p.Ser1091Thr
NM_001382788.1:c.3226T>A	NP_001369717.1:p.Ser1076Thr
NM_001382789.1:c.3217T>A	NP_001369718.1:p.Ser1073Thr
NM_001382790.1:c.3193T>A	NP_001369719.1:p.Ser1065Thr
NM_001382791.1:c.3187T>A	NP_001369720.1:p.Ser1063Thr
NM_001382792.1:c.3160T>A	NP_001369721.1:p.Ser1054Thr
NM_001382793.1:c.3154T>A	NP_001369722.1:p.Ser1052Thr
NM_001382794.1:c.3154T>A	NP_001369723.1:p.Ser1052Thr
NM_001382795.1:c.3148T>A	NP_001369724.1:p.Ser1050Thr
NM_001382796.1:c.3109T>A	NP_001369725.1:p.Ser1037Thr
NM_001382797.1:c.3097T>A	NP_001369726.1:p.Ser1033Thr
NM_001382798.1:c.3040T>A	NP_001369727.1:p.Ser1014Thr
NM_001382799.1:c.3016T>A	NP_001369728.1:p.Ser1006Thr
NM_001382800.1:c.3010T>A	NP_001369729.1:p.Ser1004Thr
NM_001382801.1:c.2992T>A	NP_001369730.1:p.Ser998Thr
NM_001382802.1:c.2938T>A	NP_001369731.1:p.Ser980Thr
NM_001382803.1:c.3117+328T>A	NP_001369732.1:n.3117+328T>A
NM_001382804.1:c.2368T>A	NP_001369733.1:p.Ser790Thr
NM_001382805.1:c.2245T>A	NP_001369734.1:p.Ser749Thr
NM_001382806.1:c.2158T>A	NP_001369735.1:p.Ser720Thr
NM_004448.4:c.3196T>A MANE Select	NP_004439.2:p.Ser1066Thr
NR_110535.2:n.3434T>A