Canonical Allele Identifier: CA399313600

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143302349
• MyVariant Identifiers: chr17:g.37884091G>T (hg19) ; chr17:g.39727838G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727838G>T , CM000679.2:g.39727838G>T	GRCh38
NC_000017.10:g.37884091G>T , CM000679.1:g.37884091G>T	GRCh37
NC_000017.9:g.35137617G>T	NCBI36
NG_007503.1:g.44699G>T , LRG_724:g.44699G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3562G>T MANE Select	ENSP00000269571.4:p.Gly1188Trp
ENST00000269571.9:c.3562G>T	ENSP00000269571.4:p.Gly1188Trp
ENST00000406381.6:c.3472G>T	ENSP00000385185.2:p.Gly1158Trp
ENST00000445658.6:c.2734G>T	ENSP00000404047.2:p.Gly912Trp
ENST00000541774.5:c.3517G>T	ENSP00000446466.1:p.Gly1173Trp
ENST00000578373.5:c.*3352G>T	ENSP00000463427.1:n.*3352G>T
ENST00000584450.5:c.*141G>T	ENSP00000463714.1:n.*141G>T
ENST00000584601.5:c.3472G>T	ENSP00000462438.1:p.Gly1158Trp
NM_001005862.2:c.3472G>T , LRG_724t1:c.3472G>T	NP_001005862.1:p.Gly1158Trp
NM_001289936.1:c.3517G>T , LRG_724t4:c.3517G>T	NP_001276865.1:p.Gly1173Trp
NM_001289937.1:c.*141G>T	NP_001276866.1:n.*141G>T
NM_004448.3:c.3562G>T , LRG_724t2:c.3562G>T	NP_004439.2:p.Gly1188Trp
NR_110535.1:n.3886G>T
XM_024450641.1:c.3700G>T	XP_024306409.1:p.Gly1234Trp
XM_024450642.1:c.3655G>T	XP_024306410.1:p.Gly1219Trp
XM_024450643.1:c.3610G>T	XP_024306411.1:p.Gly1204Trp
NM_001005862.3:c.3472G>T	NP_001005862.1:p.Gly1158Trp
NM_001289936.2:c.3517G>T	NP_001276865.1:p.Gly1173Trp
NM_001289937.2:c.*141G>T	NP_001276866.1:n.*141G>T
NM_001382782.1:c.3472G>T	NP_001369711.1:p.Gly1158Trp
NM_001382783.1:c.3472G>T	NP_001369712.1:p.Gly1158Trp
NM_001382784.1:c.3679G>T	NP_001369713.1:p.Gly1227Trp
NM_001382785.1:c.3664G>T	NP_001369714.1:p.Gly1222Trp
NM_001382786.1:c.3643G>T	NP_001369715.1:p.Gly1215Trp
NM_001382787.1:c.3637G>T	NP_001369716.1:p.Gly1213Trp
NM_001382788.1:c.3592G>T	NP_001369717.1:p.Gly1198Trp
NM_001382789.1:c.3583G>T	NP_001369718.1:p.Gly1195Trp
NM_001382790.1:c.3559G>T	NP_001369719.1:p.Gly1187Trp
NM_001382791.1:c.3553G>T	NP_001369720.1:p.Gly1185Trp
NM_001382792.1:c.3526G>T	NP_001369721.1:p.Gly1176Trp
NM_001382793.1:c.3520G>T	NP_001369722.1:p.Gly1174Trp
NM_001382794.1:c.3520G>T	NP_001369723.1:p.Gly1174Trp
NM_001382795.1:c.3514G>T	NP_001369724.1:p.Gly1172Trp
NM_001382796.1:c.3475G>T	NP_001369725.1:p.Gly1159Trp
NM_001382797.1:c.3463G>T	NP_001369726.1:p.Gly1155Trp
NM_001382798.1:c.3406G>T	NP_001369727.1:p.Gly1136Trp
NM_001382799.1:c.3382G>T	NP_001369728.1:p.Gly1128Trp
NM_001382800.1:c.3376G>T	NP_001369729.1:p.Gly1126Trp
NM_001382801.1:c.3358G>T	NP_001369730.1:p.Gly1120Trp
NM_001382802.1:c.3304G>T	NP_001369731.1:p.Gly1102Trp
NM_001382803.1:c.*141G>T	NP_001369732.1:n.*141G>T
NM_001382804.1:c.2734G>T	NP_001369733.1:p.Gly912Trp
NM_001382805.1:c.2611G>T	NP_001369734.1:p.Gly871Trp
NM_001382806.1:c.2524G>T	NP_001369735.1:p.Gly842Trp
NM_004448.4:c.3562G>T MANE Select	NP_004439.2:p.Gly1188Trp
NR_110535.2:n.3800G>T