Canonical Allele Identifier: CA399310764

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143246854
• MyVariant Identifiers: chr17:g.37883678G>C (hg19) ; chr17:g.39727425G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727425G>C , CM000679.2:g.39727425G>C	GRCh38
NC_000017.10:g.37883678G>C , CM000679.1:g.37883678G>C	GRCh37
NC_000017.9:g.35137204G>C	NCBI36
NG_007503.1:g.44286G>C , LRG_724:g.44286G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3290G>C MANE Select	ENSP00000269571.4:p.Gly1097Ala
ENST00000269571.9:c.3290G>C	ENSP00000269571.4:p.Gly1097Ala
ENST00000406381.6:c.3200G>C	ENSP00000385185.2:p.Gly1067Ala
ENST00000445658.6:c.2462G>C	ENSP00000404047.2:p.Gly821Ala
ENST00000541774.5:c.3245G>C	ENSP00000446466.1:p.Gly1082Ala
ENST00000578373.5:c.*3080G>C	ENSP00000463427.1:n.*3080G>C
ENST00000584450.5:c.3160-264G>C	ENSP00000463714.1:n.3160-264G>C
ENST00000584601.5:c.3200G>C	ENSP00000462438.1:p.Gly1067Ala
NM_001005862.2:c.3200G>C , LRG_724t1:c.3200G>C	NP_001005862.1:p.Gly1067Ala
NM_001289936.1:c.3245G>C , LRG_724t4:c.3245G>C	NP_001276865.1:p.Gly1082Ala
NM_001289937.1:c.3160-264G>C	NP_001276866.1:n.3160-264G>C
NM_004448.3:c.3290G>C , LRG_724t2:c.3290G>C	NP_004439.2:p.Gly1097Ala
NR_110535.1:n.3614G>C
XM_024450641.1:c.3428G>C	XP_024306409.1:p.Gly1143Ala
XM_024450642.1:c.3383G>C	XP_024306410.1:p.Gly1128Ala
XM_024450643.1:c.3338G>C	XP_024306411.1:p.Gly1113Ala
NM_001005862.3:c.3200G>C	NP_001005862.1:p.Gly1067Ala
NM_001289936.2:c.3245G>C	NP_001276865.1:p.Gly1082Ala
NM_001289937.2:c.3160-264G>C	NP_001276866.1:n.3160-264G>C
NM_001382782.1:c.3200G>C	NP_001369711.1:p.Gly1067Ala
NM_001382783.1:c.3200G>C	NP_001369712.1:p.Gly1067Ala
NM_001382784.1:c.3407G>C	NP_001369713.1:p.Gly1136Ala
NM_001382785.1:c.3392G>C	NP_001369714.1:p.Gly1131Ala
NM_001382786.1:c.3371G>C	NP_001369715.1:p.Gly1124Ala
NM_001382787.1:c.3365G>C	NP_001369716.1:p.Gly1122Ala
NM_001382788.1:c.3320G>C	NP_001369717.1:p.Gly1107Ala
NM_001382789.1:c.3311G>C	NP_001369718.1:p.Gly1104Ala
NM_001382790.1:c.3287G>C	NP_001369719.1:p.Gly1096Ala
NM_001382791.1:c.3281G>C	NP_001369720.1:p.Gly1094Ala
NM_001382792.1:c.3254G>C	NP_001369721.1:p.Gly1085Ala
NM_001382793.1:c.3248G>C	NP_001369722.1:p.Gly1083Ala
NM_001382794.1:c.3248G>C	NP_001369723.1:p.Gly1083Ala
NM_001382795.1:c.3242G>C	NP_001369724.1:p.Gly1081Ala
NM_001382796.1:c.3203G>C	NP_001369725.1:p.Gly1068Ala
NM_001382797.1:c.3191G>C	NP_001369726.1:p.Gly1064Ala
NM_001382798.1:c.3134G>C	NP_001369727.1:p.Gly1045Ala
NM_001382799.1:c.3110G>C	NP_001369728.1:p.Gly1037Ala
NM_001382800.1:c.3104G>C	NP_001369729.1:p.Gly1035Ala
NM_001382801.1:c.3086G>C	NP_001369730.1:p.Gly1029Ala
NM_001382802.1:c.3032G>C	NP_001369731.1:p.Gly1011Ala
NM_001382803.1:c.3118-264G>C	NP_001369732.1:n.3118-264G>C
NM_001382804.1:c.2462G>C	NP_001369733.1:p.Gly821Ala
NM_001382805.1:c.2339G>C	NP_001369734.1:p.Gly780Ala
NM_001382806.1:c.2252G>C	NP_001369735.1:p.Gly751Ala
NM_004448.4:c.3290G>C MANE Select	NP_004439.2:p.Gly1097Ala
NR_110535.2:n.3528G>C