Canonical Allele Identifier: CA399312770

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143260187
• MyVariant Identifiers: chr17:g.37883785T>C (hg19) ; chr17:g.39727532T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727532T>C , CM000679.2:g.39727532T>C	GRCh38
NC_000017.10:g.37883785T>C , CM000679.1:g.37883785T>C	GRCh37
NC_000017.9:g.35137311T>C	NCBI36
NG_007503.1:g.44393T>C , LRG_724:g.44393T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3397T>C MANE Select	ENSP00000269571.4:p.Cys1133Arg
ENST00000269571.9:c.3397T>C	ENSP00000269571.4:p.Cys1133Arg
ENST00000406381.6:c.3307T>C	ENSP00000385185.2:p.Cys1103Arg
ENST00000445658.6:c.2569T>C	ENSP00000404047.2:p.Cys857Arg
ENST00000541774.5:c.3352T>C	ENSP00000446466.1:p.Cys1118Arg
ENST00000578373.5:c.*3187T>C	ENSP00000463427.1:n.*3187T>C
ENST00000584450.5:c.3160-157T>C	ENSP00000463714.1:n.3160-157T>C
ENST00000584601.5:c.3307T>C	ENSP00000462438.1:p.Cys1103Arg
NM_001005862.2:c.3307T>C , LRG_724t1:c.3307T>C	NP_001005862.1:p.Cys1103Arg
NM_001289936.1:c.3352T>C , LRG_724t4:c.3352T>C	NP_001276865.1:p.Cys1118Arg
NM_001289937.1:c.3160-157T>C	NP_001276866.1:n.3160-157T>C
NM_004448.3:c.3397T>C , LRG_724t2:c.3397T>C	NP_004439.2:p.Cys1133Arg
NR_110535.1:n.3721T>C
XM_024450641.1:c.3535T>C	XP_024306409.1:p.Cys1179Arg
XM_024450642.1:c.3490T>C	XP_024306410.1:p.Cys1164Arg
XM_024450643.1:c.3445T>C	XP_024306411.1:p.Cys1149Arg
NM_001005862.3:c.3307T>C	NP_001005862.1:p.Cys1103Arg
NM_001289936.2:c.3352T>C	NP_001276865.1:p.Cys1118Arg
NM_001289937.2:c.3160-157T>C	NP_001276866.1:n.3160-157T>C
NM_001382782.1:c.3307T>C	NP_001369711.1:p.Cys1103Arg
NM_001382783.1:c.3307T>C	NP_001369712.1:p.Cys1103Arg
NM_001382784.1:c.3514T>C	NP_001369713.1:p.Cys1172Arg
NM_001382785.1:c.3499T>C	NP_001369714.1:p.Cys1167Arg
NM_001382786.1:c.3478T>C	NP_001369715.1:p.Cys1160Arg
NM_001382787.1:c.3472T>C	NP_001369716.1:p.Cys1158Arg
NM_001382788.1:c.3427T>C	NP_001369717.1:p.Cys1143Arg
NM_001382789.1:c.3418T>C	NP_001369718.1:p.Cys1140Arg
NM_001382790.1:c.3394T>C	NP_001369719.1:p.Cys1132Arg
NM_001382791.1:c.3388T>C	NP_001369720.1:p.Cys1130Arg
NM_001382792.1:c.3361T>C	NP_001369721.1:p.Cys1121Arg
NM_001382793.1:c.3355T>C	NP_001369722.1:p.Cys1119Arg
NM_001382794.1:c.3355T>C	NP_001369723.1:p.Cys1119Arg
NM_001382795.1:c.3349T>C	NP_001369724.1:p.Cys1117Arg
NM_001382796.1:c.3310T>C	NP_001369725.1:p.Cys1104Arg
NM_001382797.1:c.3298T>C	NP_001369726.1:p.Cys1100Arg
NM_001382798.1:c.3241T>C	NP_001369727.1:p.Cys1081Arg
NM_001382799.1:c.3217T>C	NP_001369728.1:p.Cys1073Arg
NM_001382800.1:c.3211T>C	NP_001369729.1:p.Cys1071Arg
NM_001382801.1:c.3193T>C	NP_001369730.1:p.Cys1065Arg
NM_001382802.1:c.3139T>C	NP_001369731.1:p.Cys1047Arg
NM_001382803.1:c.3118-157T>C	NP_001369732.1:n.3118-157T>C
NM_001382804.1:c.2569T>C	NP_001369733.1:p.Cys857Arg
NM_001382805.1:c.2446T>C	NP_001369734.1:p.Cys816Arg
NM_001382806.1:c.2359T>C	NP_001369735.1:p.Cys787Arg
NM_004448.4:c.3397T>C MANE Select	NP_004439.2:p.Cys1133Arg
NR_110535.2:n.3635T>C