Canonical Allele Identifier: CA399313192

Gene: ERBB2

Linked Data

• dbSNP Id: rs769120310
• MyVariant Identifiers: chr17:g.37884036G>C (hg19) ; chr17:g.39727783G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727783G>C , CM000679.2:g.39727783G>C	GRCh38
NC_000017.10:g.37884036G>C , CM000679.1:g.37884036G>C	GRCh37
NC_000017.9:g.35137562G>C	NCBI36
NG_007503.1:g.44644G>C , LRG_724:g.44644G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3507G>C MANE Select	ENSP00000269571.4:p.Arg1169Ser
ENST00000269571.9:c.3507G>C	ENSP00000269571.4:p.Arg1169Ser
ENST00000406381.6:c.3417G>C	ENSP00000385185.2:p.Arg1139Ser
ENST00000445658.6:c.2679G>C	ENSP00000404047.2:p.Arg893Ser
ENST00000541774.5:c.3462G>C	ENSP00000446466.1:p.Arg1154Ser
ENST00000578373.5:c.*3297G>C	ENSP00000463427.1:n.*3297G>C
ENST00000584450.5:c.*86G>C	ENSP00000463714.1:n.*86G>C
ENST00000584601.5:c.3417G>C	ENSP00000462438.1:p.Arg1139Ser
NM_001005862.2:c.3417G>C , LRG_724t1:c.3417G>C	NP_001005862.1:p.Arg1139Ser
NM_001289936.1:c.3462G>C , LRG_724t4:c.3462G>C	NP_001276865.1:p.Arg1154Ser
NM_001289937.1:c.*86G>C	NP_001276866.1:n.*86G>C
NM_004448.3:c.3507G>C , LRG_724t2:c.3507G>C	NP_004439.2:p.Arg1169Ser
NR_110535.1:n.3831G>C
XM_024450641.1:c.3645G>C	XP_024306409.1:p.Arg1215Ser
XM_024450642.1:c.3600G>C	XP_024306410.1:p.Arg1200Ser
XM_024450643.1:c.3555G>C	XP_024306411.1:p.Arg1185Ser
NM_001005862.3:c.3417G>C	NP_001005862.1:p.Arg1139Ser
NM_001289936.2:c.3462G>C	NP_001276865.1:p.Arg1154Ser
NM_001289937.2:c.*86G>C	NP_001276866.1:n.*86G>C
NM_001382782.1:c.3417G>C	NP_001369711.1:p.Arg1139Ser
NM_001382783.1:c.3417G>C	NP_001369712.1:p.Arg1139Ser
NM_001382784.1:c.3624G>C	NP_001369713.1:p.Arg1208Ser
NM_001382785.1:c.3609G>C	NP_001369714.1:p.Arg1203Ser
NM_001382786.1:c.3588G>C	NP_001369715.1:p.Arg1196Ser
NM_001382787.1:c.3582G>C	NP_001369716.1:p.Arg1194Ser
NM_001382788.1:c.3537G>C	NP_001369717.1:p.Arg1179Ser
NM_001382789.1:c.3528G>C	NP_001369718.1:p.Arg1176Ser
NM_001382790.1:c.3504G>C	NP_001369719.1:p.Arg1168Ser
NM_001382791.1:c.3498G>C	NP_001369720.1:p.Arg1166Ser
NM_001382792.1:c.3471G>C	NP_001369721.1:p.Arg1157Ser
NM_001382793.1:c.3465G>C	NP_001369722.1:p.Arg1155Ser
NM_001382794.1:c.3465G>C	NP_001369723.1:p.Arg1155Ser
NM_001382795.1:c.3459G>C	NP_001369724.1:p.Arg1153Ser
NM_001382796.1:c.3420G>C	NP_001369725.1:p.Arg1140Ser
NM_001382797.1:c.3408G>C	NP_001369726.1:p.Arg1136Ser
NM_001382798.1:c.3351G>C	NP_001369727.1:p.Arg1117Ser
NM_001382799.1:c.3327G>C	NP_001369728.1:p.Arg1109Ser
NM_001382800.1:c.3321G>C	NP_001369729.1:p.Arg1107Ser
NM_001382801.1:c.3303G>C	NP_001369730.1:p.Arg1101Ser
NM_001382802.1:c.3249G>C	NP_001369731.1:p.Arg1083Ser
NM_001382803.1:c.*86G>C	NP_001369732.1:n.*86G>C
NM_001382804.1:c.2679G>C	NP_001369733.1:p.Arg893Ser
NM_001382805.1:c.2556G>C	NP_001369734.1:p.Arg852Ser
NM_001382806.1:c.2469G>C	NP_001369735.1:p.Arg823Ser
NM_004448.4:c.3507G>C MANE Select	NP_004439.2:p.Arg1169Ser
NR_110535.2:n.3745G>C