Canonical Allele Identifier: CA399313330

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143298101
• MyVariant Identifiers: chr17:g.37884055G>T (hg19) ; chr17:g.39727802G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727802G>T , CM000679.2:g.39727802G>T	GRCh38
NC_000017.10:g.37884055G>T , CM000679.1:g.37884055G>T	GRCh37
NC_000017.9:g.35137581G>T	NCBI36
NG_007503.1:g.44663G>T , LRG_724:g.44663G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3526G>T MANE Select	ENSP00000269571.4:p.Gly1176Trp
ENST00000269571.9:c.3526G>T	ENSP00000269571.4:p.Gly1176Trp
ENST00000406381.6:c.3436G>T	ENSP00000385185.2:p.Gly1146Trp
ENST00000445658.6:c.2698G>T	ENSP00000404047.2:p.Gly900Trp
ENST00000541774.5:c.3481G>T	ENSP00000446466.1:p.Gly1161Trp
ENST00000578373.5:c.*3316G>T	ENSP00000463427.1:n.*3316G>T
ENST00000584450.5:c.*105G>T	ENSP00000463714.1:n.*105G>T
ENST00000584601.5:c.3436G>T	ENSP00000462438.1:p.Gly1146Trp
NM_001005862.2:c.3436G>T , LRG_724t1:c.3436G>T	NP_001005862.1:p.Gly1146Trp
NM_001289936.1:c.3481G>T , LRG_724t4:c.3481G>T	NP_001276865.1:p.Gly1161Trp
NM_001289937.1:c.*105G>T	NP_001276866.1:n.*105G>T
NM_004448.3:c.3526G>T , LRG_724t2:c.3526G>T	NP_004439.2:p.Gly1176Trp
NR_110535.1:n.3850G>T
XM_024450641.1:c.3664G>T	XP_024306409.1:p.Gly1222Trp
XM_024450642.1:c.3619G>T	XP_024306410.1:p.Gly1207Trp
XM_024450643.1:c.3574G>T	XP_024306411.1:p.Gly1192Trp
NM_001005862.3:c.3436G>T	NP_001005862.1:p.Gly1146Trp
NM_001289936.2:c.3481G>T	NP_001276865.1:p.Gly1161Trp
NM_001289937.2:c.*105G>T	NP_001276866.1:n.*105G>T
NM_001382782.1:c.3436G>T	NP_001369711.1:p.Gly1146Trp
NM_001382783.1:c.3436G>T	NP_001369712.1:p.Gly1146Trp
NM_001382784.1:c.3643G>T	NP_001369713.1:p.Gly1215Trp
NM_001382785.1:c.3628G>T	NP_001369714.1:p.Gly1210Trp
NM_001382786.1:c.3607G>T	NP_001369715.1:p.Gly1203Trp
NM_001382787.1:c.3601G>T	NP_001369716.1:p.Gly1201Trp
NM_001382788.1:c.3556G>T	NP_001369717.1:p.Gly1186Trp
NM_001382789.1:c.3547G>T	NP_001369718.1:p.Gly1183Trp
NM_001382790.1:c.3523G>T	NP_001369719.1:p.Gly1175Trp
NM_001382791.1:c.3517G>T	NP_001369720.1:p.Gly1173Trp
NM_001382792.1:c.3490G>T	NP_001369721.1:p.Gly1164Trp
NM_001382793.1:c.3484G>T	NP_001369722.1:p.Gly1162Trp
NM_001382794.1:c.3484G>T	NP_001369723.1:p.Gly1162Trp
NM_001382795.1:c.3478G>T	NP_001369724.1:p.Gly1160Trp
NM_001382796.1:c.3439G>T	NP_001369725.1:p.Gly1147Trp
NM_001382797.1:c.3427G>T	NP_001369726.1:p.Gly1143Trp
NM_001382798.1:c.3370G>T	NP_001369727.1:p.Gly1124Trp
NM_001382799.1:c.3346G>T	NP_001369728.1:p.Gly1116Trp
NM_001382800.1:c.3340G>T	NP_001369729.1:p.Gly1114Trp
NM_001382801.1:c.3322G>T	NP_001369730.1:p.Gly1108Trp
NM_001382802.1:c.3268G>T	NP_001369731.1:p.Gly1090Trp
NM_001382803.1:c.*105G>T	NP_001369732.1:n.*105G>T
NM_001382804.1:c.2698G>T	NP_001369733.1:p.Gly900Trp
NM_001382805.1:c.2575G>T	NP_001369734.1:p.Gly859Trp
NM_001382806.1:c.2488G>T	NP_001369735.1:p.Gly830Trp
NM_004448.4:c.3526G>T MANE Select	NP_004439.2:p.Gly1176Trp
NR_110535.2:n.3764G>T