Canonical Allele Identifier: CA399312865

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143288468
• MyVariant Identifiers: chr17:g.37883963T>A (hg19) ; chr17:g.39727710T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727710T>A , CM000679.2:g.39727710T>A	GRCh38
NC_000017.10:g.37883963T>A , CM000679.1:g.37883963T>A	GRCh37
NC_000017.9:g.35137489T>A	NCBI36
NG_007503.1:g.44571T>A , LRG_724:g.44571T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3434T>A MANE Select	ENSP00000269571.4:p.Val1145Asp
ENST00000269571.9:c.3434T>A	ENSP00000269571.4:p.Val1145Asp
ENST00000406381.6:c.3344T>A	ENSP00000385185.2:p.Val1115Asp
ENST00000445658.6:c.2606T>A	ENSP00000404047.2:p.Val869Asp
ENST00000541774.5:c.3389T>A	ENSP00000446466.1:p.Val1130Asp
ENST00000578373.5:c.*3224T>A	ENSP00000463427.1:n.*3224T>A
ENST00000584450.5:c.*13T>A	ENSP00000463714.1:n.*13T>A
ENST00000584601.5:c.3344T>A	ENSP00000462438.1:p.Val1115Asp
NM_001005862.2:c.3344T>A , LRG_724t1:c.3344T>A	NP_001005862.1:p.Val1115Asp
NM_001289936.1:c.3389T>A , LRG_724t4:c.3389T>A	NP_001276865.1:p.Val1130Asp
NM_001289937.1:c.*13T>A	NP_001276866.1:n.*13T>A
NM_004448.3:c.3434T>A , LRG_724t2:c.3434T>A	NP_004439.2:p.Val1145Asp
NR_110535.1:n.3758T>A
XM_024450641.1:c.3572T>A	XP_024306409.1:p.Val1191Asp
XM_024450642.1:c.3527T>A	XP_024306410.1:p.Val1176Asp
XM_024450643.1:c.3482T>A	XP_024306411.1:p.Val1161Asp
NM_001005862.3:c.3344T>A	NP_001005862.1:p.Val1115Asp
NM_001289936.2:c.3389T>A	NP_001276865.1:p.Val1130Asp
NM_001289937.2:c.*13T>A	NP_001276866.1:n.*13T>A
NM_001382782.1:c.3344T>A	NP_001369711.1:p.Val1115Asp
NM_001382783.1:c.3344T>A	NP_001369712.1:p.Val1115Asp
NM_001382784.1:c.3551T>A	NP_001369713.1:p.Val1184Asp
NM_001382785.1:c.3536T>A	NP_001369714.1:p.Val1179Asp
NM_001382786.1:c.3515T>A	NP_001369715.1:p.Val1172Asp
NM_001382787.1:c.3509T>A	NP_001369716.1:p.Val1170Asp
NM_001382788.1:c.3464T>A	NP_001369717.1:p.Val1155Asp
NM_001382789.1:c.3455T>A	NP_001369718.1:p.Val1152Asp
NM_001382790.1:c.3431T>A	NP_001369719.1:p.Val1144Asp
NM_001382791.1:c.3425T>A	NP_001369720.1:p.Val1142Asp
NM_001382792.1:c.3398T>A	NP_001369721.1:p.Val1133Asp
NM_001382793.1:c.3392T>A	NP_001369722.1:p.Val1131Asp
NM_001382794.1:c.3392T>A	NP_001369723.1:p.Val1131Asp
NM_001382795.1:c.3386T>A	NP_001369724.1:p.Val1129Asp
NM_001382796.1:c.3347T>A	NP_001369725.1:p.Val1116Asp
NM_001382797.1:c.3335T>A	NP_001369726.1:p.Val1112Asp
NM_001382798.1:c.3278T>A	NP_001369727.1:p.Val1093Asp
NM_001382799.1:c.3254T>A	NP_001369728.1:p.Val1085Asp
NM_001382800.1:c.3248T>A	NP_001369729.1:p.Val1083Asp
NM_001382801.1:c.3230T>A	NP_001369730.1:p.Val1077Asp
NM_001382802.1:c.3176T>A	NP_001369731.1:p.Val1059Asp
NM_001382803.1:c.*13T>A	NP_001369732.1:n.*13T>A
NM_001382804.1:c.2606T>A	NP_001369733.1:p.Val869Asp
NM_001382805.1:c.2483T>A	NP_001369734.1:p.Val828Asp
NM_001382806.1:c.2396T>A	NP_001369735.1:p.Val799Asp
NM_004448.4:c.3434T>A MANE Select	NP_004439.2:p.Val1145Asp
NR_110535.2:n.3672T>A