Canonical Allele Identifier: CA399312607

Gene: ERBB2

Linked Data

• dbSNP Id: rs1252510655
• MyVariant Identifiers: chr17:g.37883733C>A (hg19) ; chr17:g.39727480C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727480C>A , CM000679.2:g.39727480C>A	GRCh38
NC_000017.10:g.37883733C>A , CM000679.1:g.37883733C>A	GRCh37
NC_000017.9:g.35137259C>A	NCBI36
NG_007503.1:g.44341C>A , LRG_724:g.44341C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3345C>A MANE Select	ENSP00000269571.4:p.Asp1115Glu
ENST00000269571.9:c.3345C>A	ENSP00000269571.4:p.Asp1115Glu
ENST00000406381.6:c.3255C>A	ENSP00000385185.2:p.Asp1085Glu
ENST00000445658.6:c.2517C>A	ENSP00000404047.2:p.Asp839Glu
ENST00000541774.5:c.3300C>A	ENSP00000446466.1:p.Asp1100Glu
ENST00000578373.5:c.*3135C>A	ENSP00000463427.1:n.*3135C>A
ENST00000584450.5:c.3160-209C>A	ENSP00000463714.1:n.3160-209C>A
ENST00000584601.5:c.3255C>A	ENSP00000462438.1:p.Asp1085Glu
NM_001005862.2:c.3255C>A , LRG_724t1:c.3255C>A	NP_001005862.1:p.Asp1085Glu
NM_001289936.1:c.3300C>A , LRG_724t4:c.3300C>A	NP_001276865.1:p.Asp1100Glu
NM_001289937.1:c.3160-209C>A	NP_001276866.1:n.3160-209C>A
NM_004448.3:c.3345C>A , LRG_724t2:c.3345C>A	NP_004439.2:p.Asp1115Glu
NR_110535.1:n.3669C>A
XM_024450641.1:c.3483C>A	XP_024306409.1:p.Asp1161Glu
XM_024450642.1:c.3438C>A	XP_024306410.1:p.Asp1146Glu
XM_024450643.1:c.3393C>A	XP_024306411.1:p.Asp1131Glu
NM_001005862.3:c.3255C>A	NP_001005862.1:p.Asp1085Glu
NM_001289936.2:c.3300C>A	NP_001276865.1:p.Asp1100Glu
NM_001289937.2:c.3160-209C>A	NP_001276866.1:n.3160-209C>A
NM_001382782.1:c.3255C>A	NP_001369711.1:p.Asp1085Glu
NM_001382783.1:c.3255C>A	NP_001369712.1:p.Asp1085Glu
NM_001382784.1:c.3462C>A	NP_001369713.1:p.Asp1154Glu
NM_001382785.1:c.3447C>A	NP_001369714.1:p.Asp1149Glu
NM_001382786.1:c.3426C>A	NP_001369715.1:p.Asp1142Glu
NM_001382787.1:c.3420C>A	NP_001369716.1:p.Asp1140Glu
NM_001382788.1:c.3375C>A	NP_001369717.1:p.Asp1125Glu
NM_001382789.1:c.3366C>A	NP_001369718.1:p.Asp1122Glu
NM_001382790.1:c.3342C>A	NP_001369719.1:p.Asp1114Glu
NM_001382791.1:c.3336C>A	NP_001369720.1:p.Asp1112Glu
NM_001382792.1:c.3309C>A	NP_001369721.1:p.Asp1103Glu
NM_001382793.1:c.3303C>A	NP_001369722.1:p.Asp1101Glu
NM_001382794.1:c.3303C>A	NP_001369723.1:p.Asp1101Glu
NM_001382795.1:c.3297C>A	NP_001369724.1:p.Asp1099Glu
NM_001382796.1:c.3258C>A	NP_001369725.1:p.Asp1086Glu
NM_001382797.1:c.3246C>A	NP_001369726.1:p.Asp1082Glu
NM_001382798.1:c.3189C>A	NP_001369727.1:p.Asp1063Glu
NM_001382799.1:c.3165C>A	NP_001369728.1:p.Asp1055Glu
NM_001382800.1:c.3159C>A	NP_001369729.1:p.Asp1053Glu
NM_001382801.1:c.3141C>A	NP_001369730.1:p.Asp1047Glu
NM_001382802.1:c.3087C>A	NP_001369731.1:p.Asp1029Glu
NM_001382803.1:c.3118-209C>A	NP_001369732.1:n.3118-209C>A
NM_001382804.1:c.2517C>A	NP_001369733.1:p.Asp839Glu
NM_001382805.1:c.2394C>A	NP_001369734.1:p.Asp798Glu
NM_001382806.1:c.2307C>A	NP_001369735.1:p.Asp769Glu
NM_004448.4:c.3345C>A MANE Select	NP_004439.2:p.Asp1115Glu
NR_110535.2:n.3583C>A