Canonical Allele Identifier: CA399312692

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143255862
• MyVariant Identifiers: chr17:g.37883757G>C (hg19) ; chr17:g.39727504G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727504G>C , CM000679.2:g.39727504G>C	GRCh38
NC_000017.10:g.37883757G>C , CM000679.1:g.37883757G>C	GRCh37
NC_000017.9:g.35137283G>C	NCBI36
NG_007503.1:g.44365G>C , LRG_724:g.44365G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3369G>C MANE Select	ENSP00000269571.4:p.Glu1123Asp
ENST00000269571.9:c.3369G>C	ENSP00000269571.4:p.Glu1123Asp
ENST00000406381.6:c.3279G>C	ENSP00000385185.2:p.Glu1093Asp
ENST00000445658.6:c.2541G>C	ENSP00000404047.2:p.Glu847Asp
ENST00000541774.5:c.3324G>C	ENSP00000446466.1:p.Glu1108Asp
ENST00000578373.5:c.*3159G>C	ENSP00000463427.1:n.*3159G>C
ENST00000584450.5:c.3160-185G>C	ENSP00000463714.1:n.3160-185G>C
ENST00000584601.5:c.3279G>C	ENSP00000462438.1:p.Glu1093Asp
NM_001005862.2:c.3279G>C , LRG_724t1:c.3279G>C	NP_001005862.1:p.Glu1093Asp
NM_001289936.1:c.3324G>C , LRG_724t4:c.3324G>C	NP_001276865.1:p.Glu1108Asp
NM_001289937.1:c.3160-185G>C	NP_001276866.1:n.3160-185G>C
NM_004448.3:c.3369G>C , LRG_724t2:c.3369G>C	NP_004439.2:p.Glu1123Asp
NR_110535.1:n.3693G>C
XM_024450641.1:c.3507G>C	XP_024306409.1:p.Glu1169Asp
XM_024450642.1:c.3462G>C	XP_024306410.1:p.Glu1154Asp
XM_024450643.1:c.3417G>C	XP_024306411.1:p.Glu1139Asp
NM_001005862.3:c.3279G>C	NP_001005862.1:p.Glu1093Asp
NM_001289936.2:c.3324G>C	NP_001276865.1:p.Glu1108Asp
NM_001289937.2:c.3160-185G>C	NP_001276866.1:n.3160-185G>C
NM_001382782.1:c.3279G>C	NP_001369711.1:p.Glu1093Asp
NM_001382783.1:c.3279G>C	NP_001369712.1:p.Glu1093Asp
NM_001382784.1:c.3486G>C	NP_001369713.1:p.Glu1162Asp
NM_001382785.1:c.3471G>C	NP_001369714.1:p.Glu1157Asp
NM_001382786.1:c.3450G>C	NP_001369715.1:p.Glu1150Asp
NM_001382787.1:c.3444G>C	NP_001369716.1:p.Glu1148Asp
NM_001382788.1:c.3399G>C	NP_001369717.1:p.Glu1133Asp
NM_001382789.1:c.3390G>C	NP_001369718.1:p.Glu1130Asp
NM_001382790.1:c.3366G>C	NP_001369719.1:p.Glu1122Asp
NM_001382791.1:c.3360G>C	NP_001369720.1:p.Glu1120Asp
NM_001382792.1:c.3333G>C	NP_001369721.1:p.Glu1111Asp
NM_001382793.1:c.3327G>C	NP_001369722.1:p.Glu1109Asp
NM_001382794.1:c.3327G>C	NP_001369723.1:p.Glu1109Asp
NM_001382795.1:c.3321G>C	NP_001369724.1:p.Glu1107Asp
NM_001382796.1:c.3282G>C	NP_001369725.1:p.Glu1094Asp
NM_001382797.1:c.3270G>C	NP_001369726.1:p.Glu1090Asp
NM_001382798.1:c.3213G>C	NP_001369727.1:p.Glu1071Asp
NM_001382799.1:c.3189G>C	NP_001369728.1:p.Glu1063Asp
NM_001382800.1:c.3183G>C	NP_001369729.1:p.Glu1061Asp
NM_001382801.1:c.3165G>C	NP_001369730.1:p.Glu1055Asp
NM_001382802.1:c.3111G>C	NP_001369731.1:p.Glu1037Asp
NM_001382803.1:c.3118-185G>C	NP_001369732.1:n.3118-185G>C
NM_001382804.1:c.2541G>C	NP_001369733.1:p.Glu847Asp
NM_001382805.1:c.2418G>C	NP_001369734.1:p.Glu806Asp
NM_001382806.1:c.2331G>C	NP_001369735.1:p.Glu777Asp
NM_004448.4:c.3369G>C MANE Select	NP_004439.2:p.Glu1123Asp
NR_110535.2:n.3607G>C