Canonical Allele Identifier: CA399282020

Gene: ERBB2

Linked Data

• dbSNP Id: rs770903497
• MyVariant Identifiers: chr17:g.37868200C>G (hg19) ; chr17:g.39711947C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39711947C>G , CM000679.2:g.39711947C>G	GRCh38
NC_000017.10:g.37868200C>G , CM000679.1:g.37868200C>G	GRCh37
NC_000017.9:g.35121726C>G	NCBI36
NG_007503.1:g.28808C>G , LRG_724:g.28808C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.921C>G MANE Select	ENSP00000269571.4:p.Asp307Glu
ENST00000269571.9:c.921C>G	ENSP00000269571.4:p.Asp307Glu
ENST00000406381.6:c.831C>G	ENSP00000385185.2:p.Asp277Glu
ENST00000445658.6:c.93C>G	ENSP00000404047.2:p.Asp31Glu
ENST00000541774.5:c.876C>G	ENSP00000446466.1:p.Asp292Glu
ENST00000578199.5:c.831C>G	ENSP00000462808.1:p.Asp277Glu
ENST00000578373.5:c.*711C>G	ENSP00000463427.1:n.*711C>G
ENST00000578502.1:c.146C>G
ENST00000582648.5:c.245C>G	ENSP00000462024.1:p.Thr82Arg
ENST00000582788.5:n.410C>G
ENST00000583038.5:n.1613C>G
ENST00000584450.5:c.921C>G	ENSP00000463714.1:p.Asp307Glu
ENST00000584601.5:c.831C>G	ENSP00000462438.1:p.Asp277Glu
ENST00000584908.5:n.933C>G
NM_001005862.2:c.831C>G , LRG_724t1:c.831C>G	NP_001005862.1:p.Asp277Glu
NM_001289936.1:c.876C>G , LRG_724t4:c.876C>G	NP_001276865.1:p.Asp292Glu
NM_001289937.1:c.921C>G	NP_001276866.1:p.Asp307Glu
NM_001289938.1:c.831C>G , LRG_724t3:c.831C>G	NP_001276867.1:p.Asp277Glu
NM_004448.3:c.921C>G , LRG_724t2:c.921C>G	NP_004439.2:p.Asp307Glu
NR_110535.1:n.1245C>G
XM_024450641.1:c.1059C>G	XP_024306409.1:p.Asp353Glu
XM_024450642.1:c.1014C>G	XP_024306410.1:p.Asp338Glu
XM_024450643.1:c.969C>G	XP_024306411.1:p.Asp323Glu
NM_001005862.3:c.831C>G	NP_001005862.1:p.Asp277Glu
NM_001289936.2:c.876C>G	NP_001276865.1:p.Asp292Glu
NM_001289937.2:c.921C>G	NP_001276866.1:p.Asp307Glu
NM_001289938.2:c.831C>G	NP_001276867.1:p.Asp277Glu
NM_001382782.1:c.831C>G	NP_001369711.1:p.Asp277Glu
NM_001382783.1:c.831C>G	NP_001369712.1:p.Asp277Glu
NM_001382784.1:c.921C>G	NP_001369713.1:p.Asp307Glu
NM_001382785.1:c.921C>G	NP_001369714.1:p.Asp307Glu
NM_001382786.1:c.921C>G	NP_001369715.1:p.Asp307Glu
NM_001382787.1:c.996C>G	NP_001369716.1:p.Asp332Glu
NM_001382788.1:c.921C>G	NP_001369717.1:p.Asp307Glu
NM_001382789.1:c.921C>G	NP_001369718.1:p.Asp307Glu
NM_001382790.1:c.921C>G	NP_001369719.1:p.Asp307Glu
NM_001382791.1:c.912C>G	NP_001369720.1:p.Asp304Glu
NM_001382792.1:c.921C>G	NP_001369721.1:p.Asp307Glu
NM_001382793.1:c.921C>G	NP_001369722.1:p.Asp307Glu
NM_001382794.1:c.921C>G	NP_001369723.1:p.Asp307Glu
NM_001382795.1:c.921C>G	NP_001369724.1:p.Asp307Glu
NM_001382796.1:c.921C>G	NP_001369725.1:p.Asp307Glu
NM_001382797.1:c.921C>G	NP_001369726.1:p.Asp307Glu
NM_001382798.1:c.921C>G	NP_001369727.1:p.Asp307Glu
NM_001382799.1:c.741C>G	NP_001369728.1:p.Asp247Glu
NM_001382800.1:c.921C>G	NP_001369729.1:p.Asp307Glu
NM_001382801.1:c.921C>G	NP_001369730.1:p.Asp307Glu
NM_001382802.1:c.663C>G	NP_001369731.1:p.Asp221Glu
NM_001382803.1:c.921C>G	NP_001369732.1:p.Asp307Glu
NM_001382804.1:c.93C>G	NP_001369733.1:p.Asp31Glu
NM_001382805.1:c.921C>G	NP_001369734.1:p.Asp307Glu
NM_001382806.1:c.921C>G	NP_001369735.1:p.Asp307Glu
NM_004448.4:c.921C>G MANE Select	NP_004439.2:p.Asp307Glu
NR_110535.2:n.1159C>G