Canonical Allele Identifier: CA399312773

Gene: ERBB2

Linked Data

• dbSNP Id: rs1371638608
• MyVariant Identifiers: chr17:g.37883786G>T (hg19) ; chr17:g.39727533G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727533G>T , CM000679.2:g.39727533G>T	GRCh38
NC_000017.10:g.37883786G>T , CM000679.1:g.37883786G>T	GRCh37
NC_000017.9:g.35137312G>T	NCBI36
NG_007503.1:g.44394G>T , LRG_724:g.44394G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3398G>T MANE Select	ENSP00000269571.4:p.Cys1133Phe
ENST00000269571.9:c.3398G>T	ENSP00000269571.4:p.Cys1133Phe
ENST00000406381.6:c.3308G>T	ENSP00000385185.2:p.Cys1103Phe
ENST00000445658.6:c.2570G>T	ENSP00000404047.2:p.Cys857Phe
ENST00000541774.5:c.3353G>T	ENSP00000446466.1:p.Cys1118Phe
ENST00000578373.5:c.*3188G>T	ENSP00000463427.1:n.*3188G>T
ENST00000584450.5:c.3160-156G>T	ENSP00000463714.1:n.3160-156G>T
ENST00000584601.5:c.3308G>T	ENSP00000462438.1:p.Cys1103Phe
NM_001005862.2:c.3308G>T , LRG_724t1:c.3308G>T	NP_001005862.1:p.Cys1103Phe
NM_001289936.1:c.3353G>T , LRG_724t4:c.3353G>T	NP_001276865.1:p.Cys1118Phe
NM_001289937.1:c.3160-156G>T	NP_001276866.1:n.3160-156G>T
NM_004448.3:c.3398G>T , LRG_724t2:c.3398G>T	NP_004439.2:p.Cys1133Phe
NR_110535.1:n.3722G>T
XM_024450641.1:c.3536G>T	XP_024306409.1:p.Cys1179Phe
XM_024450642.1:c.3491G>T	XP_024306410.1:p.Cys1164Phe
XM_024450643.1:c.3446G>T	XP_024306411.1:p.Cys1149Phe
NM_001005862.3:c.3308G>T	NP_001005862.1:p.Cys1103Phe
NM_001289936.2:c.3353G>T	NP_001276865.1:p.Cys1118Phe
NM_001289937.2:c.3160-156G>T	NP_001276866.1:n.3160-156G>T
NM_001382782.1:c.3308G>T	NP_001369711.1:p.Cys1103Phe
NM_001382783.1:c.3308G>T	NP_001369712.1:p.Cys1103Phe
NM_001382784.1:c.3515G>T	NP_001369713.1:p.Cys1172Phe
NM_001382785.1:c.3500G>T	NP_001369714.1:p.Cys1167Phe
NM_001382786.1:c.3479G>T	NP_001369715.1:p.Cys1160Phe
NM_001382787.1:c.3473G>T	NP_001369716.1:p.Cys1158Phe
NM_001382788.1:c.3428G>T	NP_001369717.1:p.Cys1143Phe
NM_001382789.1:c.3419G>T	NP_001369718.1:p.Cys1140Phe
NM_001382790.1:c.3395G>T	NP_001369719.1:p.Cys1132Phe
NM_001382791.1:c.3389G>T	NP_001369720.1:p.Cys1130Phe
NM_001382792.1:c.3362G>T	NP_001369721.1:p.Cys1121Phe
NM_001382793.1:c.3356G>T	NP_001369722.1:p.Cys1119Phe
NM_001382794.1:c.3356G>T	NP_001369723.1:p.Cys1119Phe
NM_001382795.1:c.3350G>T	NP_001369724.1:p.Cys1117Phe
NM_001382796.1:c.3311G>T	NP_001369725.1:p.Cys1104Phe
NM_001382797.1:c.3299G>T	NP_001369726.1:p.Cys1100Phe
NM_001382798.1:c.3242G>T	NP_001369727.1:p.Cys1081Phe
NM_001382799.1:c.3218G>T	NP_001369728.1:p.Cys1073Phe
NM_001382800.1:c.3212G>T	NP_001369729.1:p.Cys1071Phe
NM_001382801.1:c.3194G>T	NP_001369730.1:p.Cys1065Phe
NM_001382802.1:c.3140G>T	NP_001369731.1:p.Cys1047Phe
NM_001382803.1:c.3118-156G>T	NP_001369732.1:n.3118-156G>T
NM_001382804.1:c.2570G>T	NP_001369733.1:p.Cys857Phe
NM_001382805.1:c.2447G>T	NP_001369734.1:p.Cys816Phe
NM_001382806.1:c.2360G>T	NP_001369735.1:p.Cys787Phe
NM_004448.4:c.3398G>T MANE Select	NP_004439.2:p.Cys1133Phe
NR_110535.2:n.3636G>T