Canonical Allele Identifier: CA399310277

Gene: ERBB2

Linked Data

• dbSNP Id: rs1029099711
• MyVariant Identifiers: chr17:g.37883595G>T (hg19) ; chr17:g.39727342G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727342G>T , CM000679.2:g.39727342G>T	GRCh38
NC_000017.10:g.37883595G>T , CM000679.1:g.37883595G>T	GRCh37
NC_000017.9:g.35137121G>T	NCBI36
NG_007503.1:g.44203G>T , LRG_724:g.44203G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3207G>T MANE Select	ENSP00000269571.4:p.Glu1069Asp
ENST00000269571.9:c.3207G>T	ENSP00000269571.4:p.Glu1069Asp
ENST00000406381.6:c.3117G>T	ENSP00000385185.2:p.Glu1039Asp
ENST00000445658.6:c.2379G>T	ENSP00000404047.2:p.Glu793Asp
ENST00000541774.5:c.3162G>T	ENSP00000446466.1:p.Glu1054Asp
ENST00000578373.5:c.*2997G>T	ENSP00000463427.1:n.*2997G>T
ENST00000584450.5:c.3159+339G>T	ENSP00000463714.1:n.3159+339G>T
ENST00000584601.5:c.3117G>T	ENSP00000462438.1:p.Glu1039Asp
NM_001005862.2:c.3117G>T , LRG_724t1:c.3117G>T	NP_001005862.1:p.Glu1039Asp
NM_001289936.1:c.3162G>T , LRG_724t4:c.3162G>T	NP_001276865.1:p.Glu1054Asp
NM_001289937.1:c.3159+339G>T	NP_001276866.1:n.3159+339G>T
NM_004448.3:c.3207G>T , LRG_724t2:c.3207G>T	NP_004439.2:p.Glu1069Asp
NR_110535.1:n.3531G>T
XM_024450641.1:c.3345G>T	XP_024306409.1:p.Glu1115Asp
XM_024450642.1:c.3300G>T	XP_024306410.1:p.Glu1100Asp
XM_024450643.1:c.3255G>T	XP_024306411.1:p.Glu1085Asp
NM_001005862.3:c.3117G>T	NP_001005862.1:p.Glu1039Asp
NM_001289936.2:c.3162G>T	NP_001276865.1:p.Glu1054Asp
NM_001289937.2:c.3159+339G>T	NP_001276866.1:n.3159+339G>T
NM_001382782.1:c.3117G>T	NP_001369711.1:p.Glu1039Asp
NM_001382783.1:c.3117G>T	NP_001369712.1:p.Glu1039Asp
NM_001382784.1:c.3324G>T	NP_001369713.1:p.Glu1108Asp
NM_001382785.1:c.3309G>T	NP_001369714.1:p.Glu1103Asp
NM_001382786.1:c.3288G>T	NP_001369715.1:p.Glu1096Asp
NM_001382787.1:c.3282G>T	NP_001369716.1:p.Glu1094Asp
NM_001382788.1:c.3237G>T	NP_001369717.1:p.Glu1079Asp
NM_001382789.1:c.3228G>T	NP_001369718.1:p.Glu1076Asp
NM_001382790.1:c.3204G>T	NP_001369719.1:p.Glu1068Asp
NM_001382791.1:c.3198G>T	NP_001369720.1:p.Glu1066Asp
NM_001382792.1:c.3171G>T	NP_001369721.1:p.Glu1057Asp
NM_001382793.1:c.3165G>T	NP_001369722.1:p.Glu1055Asp
NM_001382794.1:c.3165G>T	NP_001369723.1:p.Glu1055Asp
NM_001382795.1:c.3159G>T	NP_001369724.1:p.Glu1053Asp
NM_001382796.1:c.3120G>T	NP_001369725.1:p.Glu1040Asp
NM_001382797.1:c.3108G>T	NP_001369726.1:p.Glu1036Asp
NM_001382798.1:c.3051G>T	NP_001369727.1:p.Glu1017Asp
NM_001382799.1:c.3027G>T	NP_001369728.1:p.Glu1009Asp
NM_001382800.1:c.3021G>T	NP_001369729.1:p.Glu1007Asp
NM_001382801.1:c.3003G>T	NP_001369730.1:p.Glu1001Asp
NM_001382802.1:c.2949G>T	NP_001369731.1:p.Glu983Asp
NM_001382803.1:c.3117+339G>T	NP_001369732.1:n.3117+339G>T
NM_001382804.1:c.2379G>T	NP_001369733.1:p.Glu793Asp
NM_001382805.1:c.2256G>T	NP_001369734.1:p.Glu752Asp
NM_001382806.1:c.2169G>T	NP_001369735.1:p.Glu723Asp
NM_004448.4:c.3207G>T MANE Select	NP_004439.2:p.Glu1069Asp
NR_110535.2:n.3445G>T