Canonical Allele Identifier: CA399312688

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143255738
• MyVariant Identifiers: chr17:g.37883756A>T (hg19) ; chr17:g.39727503A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727503A>T , CM000679.2:g.39727503A>T	GRCh38
NC_000017.10:g.37883756A>T , CM000679.1:g.37883756A>T	GRCh37
NC_000017.9:g.35137282A>T	NCBI36
NG_007503.1:g.44364A>T , LRG_724:g.44364A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3368A>T MANE Select	ENSP00000269571.4:p.Glu1123Val
ENST00000269571.9:c.3368A>T	ENSP00000269571.4:p.Glu1123Val
ENST00000406381.6:c.3278A>T	ENSP00000385185.2:p.Glu1093Val
ENST00000445658.6:c.2540A>T	ENSP00000404047.2:p.Glu847Val
ENST00000541774.5:c.3323A>T	ENSP00000446466.1:p.Glu1108Val
ENST00000578373.5:c.*3158A>T	ENSP00000463427.1:n.*3158A>T
ENST00000584450.5:c.3160-186A>T	ENSP00000463714.1:n.3160-186A>T
ENST00000584601.5:c.3278A>T	ENSP00000462438.1:p.Glu1093Val
NM_001005862.2:c.3278A>T , LRG_724t1:c.3278A>T	NP_001005862.1:p.Glu1093Val
NM_001289936.1:c.3323A>T , LRG_724t4:c.3323A>T	NP_001276865.1:p.Glu1108Val
NM_001289937.1:c.3160-186A>T	NP_001276866.1:n.3160-186A>T
NM_004448.3:c.3368A>T , LRG_724t2:c.3368A>T	NP_004439.2:p.Glu1123Val
NR_110535.1:n.3692A>T
XM_024450641.1:c.3506A>T	XP_024306409.1:p.Glu1169Val
XM_024450642.1:c.3461A>T	XP_024306410.1:p.Glu1154Val
XM_024450643.1:c.3416A>T	XP_024306411.1:p.Glu1139Val
NM_001005862.3:c.3278A>T	NP_001005862.1:p.Glu1093Val
NM_001289936.2:c.3323A>T	NP_001276865.1:p.Glu1108Val
NM_001289937.2:c.3160-186A>T	NP_001276866.1:n.3160-186A>T
NM_001382782.1:c.3278A>T	NP_001369711.1:p.Glu1093Val
NM_001382783.1:c.3278A>T	NP_001369712.1:p.Glu1093Val
NM_001382784.1:c.3485A>T	NP_001369713.1:p.Glu1162Val
NM_001382785.1:c.3470A>T	NP_001369714.1:p.Glu1157Val
NM_001382786.1:c.3449A>T	NP_001369715.1:p.Glu1150Val
NM_001382787.1:c.3443A>T	NP_001369716.1:p.Glu1148Val
NM_001382788.1:c.3398A>T	NP_001369717.1:p.Glu1133Val
NM_001382789.1:c.3389A>T	NP_001369718.1:p.Glu1130Val
NM_001382790.1:c.3365A>T	NP_001369719.1:p.Glu1122Val
NM_001382791.1:c.3359A>T	NP_001369720.1:p.Glu1120Val
NM_001382792.1:c.3332A>T	NP_001369721.1:p.Glu1111Val
NM_001382793.1:c.3326A>T	NP_001369722.1:p.Glu1109Val
NM_001382794.1:c.3326A>T	NP_001369723.1:p.Glu1109Val
NM_001382795.1:c.3320A>T	NP_001369724.1:p.Glu1107Val
NM_001382796.1:c.3281A>T	NP_001369725.1:p.Glu1094Val
NM_001382797.1:c.3269A>T	NP_001369726.1:p.Glu1090Val
NM_001382798.1:c.3212A>T	NP_001369727.1:p.Glu1071Val
NM_001382799.1:c.3188A>T	NP_001369728.1:p.Glu1063Val
NM_001382800.1:c.3182A>T	NP_001369729.1:p.Glu1061Val
NM_001382801.1:c.3164A>T	NP_001369730.1:p.Glu1055Val
NM_001382802.1:c.3110A>T	NP_001369731.1:p.Glu1037Val
NM_001382803.1:c.3118-186A>T	NP_001369732.1:n.3118-186A>T
NM_001382804.1:c.2540A>T	NP_001369733.1:p.Glu847Val
NM_001382805.1:c.2417A>T	NP_001369734.1:p.Glu806Val
NM_001382806.1:c.2330A>T	NP_001369735.1:p.Glu777Val
NM_004448.4:c.3368A>T MANE Select	NP_004439.2:p.Glu1123Val
NR_110535.2:n.3606A>T