Canonical Allele Identifier: CA399312769

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3397T>A MANE Select	ENSP00000269571.4:p.Cys1133Ser
ENST00000269571.9:c.3397T>A	ENSP00000269571.4:p.Cys1133Ser
ENST00000406381.6:c.3307T>A	ENSP00000385185.2:p.Cys1103Ser
ENST00000445658.6:c.2569T>A	ENSP00000404047.2:p.Cys857Ser
ENST00000541774.5:c.3352T>A	ENSP00000446466.1:p.Cys1118Ser
ENST00000578373.5:c.*3187T>A	ENSP00000463427.1:n.*3187T>A
ENST00000584450.5:c.3160-157T>A	ENSP00000463714.1:n.3160-157T>A
ENST00000584601.5:c.3307T>A	ENSP00000462438.1:p.Cys1103Ser
NM_001005862.2:c.3307T>A , LRG_724t1:c.3307T>A	NP_001005862.1:p.Cys1103Ser
NM_001289936.1:c.3352T>A , LRG_724t4:c.3352T>A	NP_001276865.1:p.Cys1118Ser
NM_001289937.1:c.3160-157T>A	NP_001276866.1:n.3160-157T>A
NM_004448.3:c.3397T>A , LRG_724t2:c.3397T>A	NP_004439.2:p.Cys1133Ser
NR_110535.1:n.3721T>A
XM_024450641.1:c.3535T>A	XP_024306409.1:p.Cys1179Ser
XM_024450642.1:c.3490T>A	XP_024306410.1:p.Cys1164Ser
XM_024450643.1:c.3445T>A	XP_024306411.1:p.Cys1149Ser
NM_001005862.3:c.3307T>A	NP_001005862.1:p.Cys1103Ser
NM_001289936.2:c.3352T>A	NP_001276865.1:p.Cys1118Ser
NM_001289937.2:c.3160-157T>A	NP_001276866.1:n.3160-157T>A
NM_001382782.1:c.3307T>A	NP_001369711.1:p.Cys1103Ser
NM_001382783.1:c.3307T>A	NP_001369712.1:p.Cys1103Ser
NM_001382784.1:c.3514T>A	NP_001369713.1:p.Cys1172Ser
NM_001382785.1:c.3499T>A	NP_001369714.1:p.Cys1167Ser
NM_001382786.1:c.3478T>A	NP_001369715.1:p.Cys1160Ser
NM_001382787.1:c.3472T>A	NP_001369716.1:p.Cys1158Ser
NM_001382788.1:c.3427T>A	NP_001369717.1:p.Cys1143Ser
NM_001382789.1:c.3418T>A	NP_001369718.1:p.Cys1140Ser
NM_001382790.1:c.3394T>A	NP_001369719.1:p.Cys1132Ser
NM_001382791.1:c.3388T>A	NP_001369720.1:p.Cys1130Ser
NM_001382792.1:c.3361T>A	NP_001369721.1:p.Cys1121Ser
NM_001382793.1:c.3355T>A	NP_001369722.1:p.Cys1119Ser
NM_001382794.1:c.3355T>A	NP_001369723.1:p.Cys1119Ser
NM_001382795.1:c.3349T>A	NP_001369724.1:p.Cys1117Ser
NM_001382796.1:c.3310T>A	NP_001369725.1:p.Cys1104Ser
NM_001382797.1:c.3298T>A	NP_001369726.1:p.Cys1100Ser
NM_001382798.1:c.3241T>A	NP_001369727.1:p.Cys1081Ser
NM_001382799.1:c.3217T>A	NP_001369728.1:p.Cys1073Ser
NM_001382800.1:c.3211T>A	NP_001369729.1:p.Cys1071Ser
NM_001382801.1:c.3193T>A	NP_001369730.1:p.Cys1065Ser
NM_001382802.1:c.3139T>A	NP_001369731.1:p.Cys1047Ser
NM_001382803.1:c.3118-157T>A	NP_001369732.1:n.3118-157T>A
NM_001382804.1:c.2569T>A	NP_001369733.1:p.Cys857Ser
NM_001382805.1:c.2446T>A	NP_001369734.1:p.Cys816Ser
NM_001382806.1:c.2359T>A	NP_001369735.1:p.Cys787Ser
NM_004448.4:c.3397T>A MANE Select	NP_004439.2:p.Cys1133Ser
NR_110535.2:n.3635T>A