Canonical Allele Identifier: CA399313337

Gene: ERBB2

Linked Data

• ClinVar Variation Id: 2786362
• ClinVar RCV Id: RCV003666424
• dbSNP Id: rs1365431216
• gnomAD v2: 17-37884056-G-A
• gnomAD v4: 17-39727803-G-A
• MyVariant Identifiers: chr17:g.37884056G>A (hg19) ; chr17:g.39727803G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727803G>A , CM000679.2:g.39727803G>A	GRCh38
NC_000017.10:g.37884056G>A , CM000679.1:g.37884056G>A	GRCh37
NC_000017.9:g.35137582G>A	NCBI36
NG_007503.1:g.44664G>A , LRG_724:g.44664G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3527G>A MANE Select	ENSP00000269571.4:p.Gly1176Glu
ENST00000269571.9:c.3527G>A	ENSP00000269571.4:p.Gly1176Glu
ENST00000406381.6:c.3437G>A	ENSP00000385185.2:p.Gly1146Glu
ENST00000445658.6:c.2699G>A	ENSP00000404047.2:p.Gly900Glu
ENST00000541774.5:c.3482G>A	ENSP00000446466.1:p.Gly1161Glu
ENST00000578373.5:c.*3317G>A	ENSP00000463427.1:n.*3317G>A
ENST00000584450.5:c.*106G>A	ENSP00000463714.1:n.*106G>A
ENST00000584601.5:c.3437G>A	ENSP00000462438.1:p.Gly1146Glu
NM_001005862.2:c.3437G>A , LRG_724t1:c.3437G>A	NP_001005862.1:p.Gly1146Glu
NM_001289936.1:c.3482G>A , LRG_724t4:c.3482G>A	NP_001276865.1:p.Gly1161Glu
NM_001289937.1:c.*106G>A	NP_001276866.1:n.*106G>A
NM_004448.3:c.3527G>A , LRG_724t2:c.3527G>A	NP_004439.2:p.Gly1176Glu
NR_110535.1:n.3851G>A
XM_024450641.1:c.3665G>A	XP_024306409.1:p.Gly1222Glu
XM_024450642.1:c.3620G>A	XP_024306410.1:p.Gly1207Glu
XM_024450643.1:c.3575G>A	XP_024306411.1:p.Gly1192Glu
NM_001005862.3:c.3437G>A	NP_001005862.1:p.Gly1146Glu
NM_001289936.2:c.3482G>A	NP_001276865.1:p.Gly1161Glu
NM_001289937.2:c.*106G>A	NP_001276866.1:n.*106G>A
NM_001382782.1:c.3437G>A	NP_001369711.1:p.Gly1146Glu
NM_001382783.1:c.3437G>A	NP_001369712.1:p.Gly1146Glu
NM_001382784.1:c.3644G>A	NP_001369713.1:p.Gly1215Glu
NM_001382785.1:c.3629G>A	NP_001369714.1:p.Gly1210Glu
NM_001382786.1:c.3608G>A	NP_001369715.1:p.Gly1203Glu
NM_001382787.1:c.3602G>A	NP_001369716.1:p.Gly1201Glu
NM_001382788.1:c.3557G>A	NP_001369717.1:p.Gly1186Glu
NM_001382789.1:c.3548G>A	NP_001369718.1:p.Gly1183Glu
NM_001382790.1:c.3524G>A	NP_001369719.1:p.Gly1175Glu
NM_001382791.1:c.3518G>A	NP_001369720.1:p.Gly1173Glu
NM_001382792.1:c.3491G>A	NP_001369721.1:p.Gly1164Glu
NM_001382793.1:c.3485G>A	NP_001369722.1:p.Gly1162Glu
NM_001382794.1:c.3485G>A	NP_001369723.1:p.Gly1162Glu
NM_001382795.1:c.3479G>A	NP_001369724.1:p.Gly1160Glu
NM_001382796.1:c.3440G>A	NP_001369725.1:p.Gly1147Glu
NM_001382797.1:c.3428G>A	NP_001369726.1:p.Gly1143Glu
NM_001382798.1:c.3371G>A	NP_001369727.1:p.Gly1124Glu
NM_001382799.1:c.3347G>A	NP_001369728.1:p.Gly1116Glu
NM_001382800.1:c.3341G>A	NP_001369729.1:p.Gly1114Glu
NM_001382801.1:c.3323G>A	NP_001369730.1:p.Gly1108Glu
NM_001382802.1:c.3269G>A	NP_001369731.1:p.Gly1090Glu
NM_001382803.1:c.*106G>A	NP_001369732.1:n.*106G>A
NM_001382804.1:c.2699G>A	NP_001369733.1:p.Gly900Glu
NM_001382805.1:c.2576G>A	NP_001369734.1:p.Gly859Glu
NM_001382806.1:c.2489G>A	NP_001369735.1:p.Gly830Glu
NM_004448.4:c.3527G>A MANE Select	NP_004439.2:p.Gly1176Glu
NR_110535.2:n.3765G>A