Canonical Allele Identifier: CA399313658

Gene: ERBB2

Linked Data

• dbSNP Id: rs1167419546
• gnomAD v2: 17-37884100-G-A
• gnomAD v4: 17-39727847-G-A
• COSMIC: COSM5570600 ; COSM5570601
• MyVariant Identifiers: chr17:g.37884100G>A (hg19) ; chr17:g.39727847G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727847G>A , CM000679.2:g.39727847G>A	GRCh38
NC_000017.10:g.37884100G>A , CM000679.1:g.37884100G>A	GRCh37
NC_000017.9:g.35137626G>A	NCBI36
NG_007503.1:g.44708G>A , LRG_724:g.44708G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3571G>A MANE Select	ENSP00000269571.4:p.Val1191Met
ENST00000269571.9:c.3571G>A	ENSP00000269571.4:p.Val1191Met
ENST00000406381.6:c.3481G>A	ENSP00000385185.2:p.Val1161Met
ENST00000445658.6:c.2743G>A	ENSP00000404047.2:p.Val915Met
ENST00000541774.5:c.3526G>A	ENSP00000446466.1:p.Val1176Met
ENST00000578373.5:c.*3361G>A	ENSP00000463427.1:n.*3361G>A
ENST00000584450.5:c.*150G>A	ENSP00000463714.1:n.*150G>A
ENST00000584601.5:c.3481G>A	ENSP00000462438.1:p.Val1161Met
NM_001005862.2:c.3481G>A , LRG_724t1:c.3481G>A	NP_001005862.1:p.Val1161Met
NM_001289936.1:c.3526G>A , LRG_724t4:c.3526G>A	NP_001276865.1:p.Val1176Met
NM_001289937.1:c.*150G>A	NP_001276866.1:n.*150G>A
NM_004448.3:c.3571G>A , LRG_724t2:c.3571G>A	NP_004439.2:p.Val1191Met
NR_110535.1:n.3895G>A
XM_024450641.1:c.3709G>A	XP_024306409.1:p.Val1237Met
XM_024450642.1:c.3664G>A	XP_024306410.1:p.Val1222Met
XM_024450643.1:c.3619G>A	XP_024306411.1:p.Val1207Met
NM_001005862.3:c.3481G>A	NP_001005862.1:p.Val1161Met
NM_001289936.2:c.3526G>A	NP_001276865.1:p.Val1176Met
NM_001289937.2:c.*150G>A	NP_001276866.1:n.*150G>A
NM_001382782.1:c.3481G>A	NP_001369711.1:p.Val1161Met
NM_001382783.1:c.3481G>A	NP_001369712.1:p.Val1161Met
NM_001382784.1:c.3688G>A	NP_001369713.1:p.Val1230Met
NM_001382785.1:c.3673G>A	NP_001369714.1:p.Val1225Met
NM_001382786.1:c.3652G>A	NP_001369715.1:p.Val1218Met
NM_001382787.1:c.3646G>A	NP_001369716.1:p.Val1216Met
NM_001382788.1:c.3601G>A	NP_001369717.1:p.Val1201Met
NM_001382789.1:c.3592G>A	NP_001369718.1:p.Val1198Met
NM_001382790.1:c.3568G>A	NP_001369719.1:p.Val1190Met
NM_001382791.1:c.3562G>A	NP_001369720.1:p.Val1188Met
NM_001382792.1:c.3535G>A	NP_001369721.1:p.Val1179Met
NM_001382793.1:c.3529G>A	NP_001369722.1:p.Val1177Met
NM_001382794.1:c.3529G>A	NP_001369723.1:p.Val1177Met
NM_001382795.1:c.3523G>A	NP_001369724.1:p.Val1175Met
NM_001382796.1:c.3484G>A	NP_001369725.1:p.Val1162Met
NM_001382797.1:c.3472G>A	NP_001369726.1:p.Val1158Met
NM_001382798.1:c.3415G>A	NP_001369727.1:p.Val1139Met
NM_001382799.1:c.3391G>A	NP_001369728.1:p.Val1131Met
NM_001382800.1:c.3385G>A	NP_001369729.1:p.Val1129Met
NM_001382801.1:c.3367G>A	NP_001369730.1:p.Val1123Met
NM_001382802.1:c.3313G>A	NP_001369731.1:p.Val1105Met
NM_001382803.1:c.*150G>A	NP_001369732.1:n.*150G>A
NM_001382804.1:c.2743G>A	NP_001369733.1:p.Val915Met
NM_001382805.1:c.2620G>A	NP_001369734.1:p.Val874Met
NM_001382806.1:c.2533G>A	NP_001369735.1:p.Val845Met
NM_004448.4:c.3571G>A MANE Select	NP_004439.2:p.Val1191Met
NR_110535.2:n.3809G>A