Canonical Allele Identifier: CA399312866

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3434T>C MANE Select	ENSP00000269571.4:p.Val1145Ala
ENST00000269571.9:c.3434T>C	ENSP00000269571.4:p.Val1145Ala
ENST00000406381.6:c.3344T>C	ENSP00000385185.2:p.Val1115Ala
ENST00000445658.6:c.2606T>C	ENSP00000404047.2:p.Val869Ala
ENST00000541774.5:c.3389T>C	ENSP00000446466.1:p.Val1130Ala
ENST00000578373.5:c.*3224T>C	ENSP00000463427.1:n.*3224T>C
ENST00000584450.5:c.*13T>C	ENSP00000463714.1:n.*13T>C
ENST00000584601.5:c.3344T>C	ENSP00000462438.1:p.Val1115Ala
NM_001005862.2:c.3344T>C , LRG_724t1:c.3344T>C	NP_001005862.1:p.Val1115Ala
NM_001289936.1:c.3389T>C , LRG_724t4:c.3389T>C	NP_001276865.1:p.Val1130Ala
NM_001289937.1:c.*13T>C	NP_001276866.1:n.*13T>C
NM_004448.3:c.3434T>C , LRG_724t2:c.3434T>C	NP_004439.2:p.Val1145Ala
NR_110535.1:n.3758T>C
XM_024450641.1:c.3572T>C	XP_024306409.1:p.Val1191Ala
XM_024450642.1:c.3527T>C	XP_024306410.1:p.Val1176Ala
XM_024450643.1:c.3482T>C	XP_024306411.1:p.Val1161Ala
NM_001005862.3:c.3344T>C	NP_001005862.1:p.Val1115Ala
NM_001289936.2:c.3389T>C	NP_001276865.1:p.Val1130Ala
NM_001289937.2:c.*13T>C	NP_001276866.1:n.*13T>C
NM_001382782.1:c.3344T>C	NP_001369711.1:p.Val1115Ala
NM_001382783.1:c.3344T>C	NP_001369712.1:p.Val1115Ala
NM_001382784.1:c.3551T>C	NP_001369713.1:p.Val1184Ala
NM_001382785.1:c.3536T>C	NP_001369714.1:p.Val1179Ala
NM_001382786.1:c.3515T>C	NP_001369715.1:p.Val1172Ala
NM_001382787.1:c.3509T>C	NP_001369716.1:p.Val1170Ala
NM_001382788.1:c.3464T>C	NP_001369717.1:p.Val1155Ala
NM_001382789.1:c.3455T>C	NP_001369718.1:p.Val1152Ala
NM_001382790.1:c.3431T>C	NP_001369719.1:p.Val1144Ala
NM_001382791.1:c.3425T>C	NP_001369720.1:p.Val1142Ala
NM_001382792.1:c.3398T>C	NP_001369721.1:p.Val1133Ala
NM_001382793.1:c.3392T>C	NP_001369722.1:p.Val1131Ala
NM_001382794.1:c.3392T>C	NP_001369723.1:p.Val1131Ala
NM_001382795.1:c.3386T>C	NP_001369724.1:p.Val1129Ala
NM_001382796.1:c.3347T>C	NP_001369725.1:p.Val1116Ala
NM_001382797.1:c.3335T>C	NP_001369726.1:p.Val1112Ala
NM_001382798.1:c.3278T>C	NP_001369727.1:p.Val1093Ala
NM_001382799.1:c.3254T>C	NP_001369728.1:p.Val1085Ala
NM_001382800.1:c.3248T>C	NP_001369729.1:p.Val1083Ala
NM_001382801.1:c.3230T>C	NP_001369730.1:p.Val1077Ala
NM_001382802.1:c.3176T>C	NP_001369731.1:p.Val1059Ala
NM_001382803.1:c.*13T>C	NP_001369732.1:n.*13T>C
NM_001382804.1:c.2606T>C	NP_001369733.1:p.Val869Ala
NM_001382805.1:c.2483T>C	NP_001369734.1:p.Val828Ala
NM_001382806.1:c.2396T>C	NP_001369735.1:p.Val799Ala
NM_004448.4:c.3434T>C MANE Select	NP_004439.2:p.Val1145Ala
NR_110535.2:n.3672T>C