Canonical Allele Identifier: CA399312771

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3397T>G MANE Select	ENSP00000269571.4:p.Cys1133Gly
ENST00000269571.9:c.3397T>G	ENSP00000269571.4:p.Cys1133Gly
ENST00000406381.6:c.3307T>G	ENSP00000385185.2:p.Cys1103Gly
ENST00000445658.6:c.2569T>G	ENSP00000404047.2:p.Cys857Gly
ENST00000541774.5:c.3352T>G	ENSP00000446466.1:p.Cys1118Gly
ENST00000578373.5:c.*3187T>G	ENSP00000463427.1:n.*3187T>G
ENST00000584450.5:c.3160-157T>G	ENSP00000463714.1:n.3160-157T>G
ENST00000584601.5:c.3307T>G	ENSP00000462438.1:p.Cys1103Gly
NM_001005862.2:c.3307T>G , LRG_724t1:c.3307T>G	NP_001005862.1:p.Cys1103Gly
NM_001289936.1:c.3352T>G , LRG_724t4:c.3352T>G	NP_001276865.1:p.Cys1118Gly
NM_001289937.1:c.3160-157T>G	NP_001276866.1:n.3160-157T>G
NM_004448.3:c.3397T>G , LRG_724t2:c.3397T>G	NP_004439.2:p.Cys1133Gly
NR_110535.1:n.3721T>G
XM_024450641.1:c.3535T>G	XP_024306409.1:p.Cys1179Gly
XM_024450642.1:c.3490T>G	XP_024306410.1:p.Cys1164Gly
XM_024450643.1:c.3445T>G	XP_024306411.1:p.Cys1149Gly
NM_001005862.3:c.3307T>G	NP_001005862.1:p.Cys1103Gly
NM_001289936.2:c.3352T>G	NP_001276865.1:p.Cys1118Gly
NM_001289937.2:c.3160-157T>G	NP_001276866.1:n.3160-157T>G
NM_001382782.1:c.3307T>G	NP_001369711.1:p.Cys1103Gly
NM_001382783.1:c.3307T>G	NP_001369712.1:p.Cys1103Gly
NM_001382784.1:c.3514T>G	NP_001369713.1:p.Cys1172Gly
NM_001382785.1:c.3499T>G	NP_001369714.1:p.Cys1167Gly
NM_001382786.1:c.3478T>G	NP_001369715.1:p.Cys1160Gly
NM_001382787.1:c.3472T>G	NP_001369716.1:p.Cys1158Gly
NM_001382788.1:c.3427T>G	NP_001369717.1:p.Cys1143Gly
NM_001382789.1:c.3418T>G	NP_001369718.1:p.Cys1140Gly
NM_001382790.1:c.3394T>G	NP_001369719.1:p.Cys1132Gly
NM_001382791.1:c.3388T>G	NP_001369720.1:p.Cys1130Gly
NM_001382792.1:c.3361T>G	NP_001369721.1:p.Cys1121Gly
NM_001382793.1:c.3355T>G	NP_001369722.1:p.Cys1119Gly
NM_001382794.1:c.3355T>G	NP_001369723.1:p.Cys1119Gly
NM_001382795.1:c.3349T>G	NP_001369724.1:p.Cys1117Gly
NM_001382796.1:c.3310T>G	NP_001369725.1:p.Cys1104Gly
NM_001382797.1:c.3298T>G	NP_001369726.1:p.Cys1100Gly
NM_001382798.1:c.3241T>G	NP_001369727.1:p.Cys1081Gly
NM_001382799.1:c.3217T>G	NP_001369728.1:p.Cys1073Gly
NM_001382800.1:c.3211T>G	NP_001369729.1:p.Cys1071Gly
NM_001382801.1:c.3193T>G	NP_001369730.1:p.Cys1065Gly
NM_001382802.1:c.3139T>G	NP_001369731.1:p.Cys1047Gly
NM_001382803.1:c.3118-157T>G	NP_001369732.1:n.3118-157T>G
NM_001382804.1:c.2569T>G	NP_001369733.1:p.Cys857Gly
NM_001382805.1:c.2446T>G	NP_001369734.1:p.Cys816Gly
NM_001382806.1:c.2359T>G	NP_001369735.1:p.Cys787Gly
NM_004448.4:c.3397T>G MANE Select	NP_004439.2:p.Cys1133Gly
NR_110535.2:n.3635T>G