Canonical Allele Identifier: CA399313592

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39727838-G-C
• MyVariant Identifiers: chr17:g.37884091G>C (hg19) ; chr17:g.39727838G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3562G>C MANE Select	ENSP00000269571.4:p.Gly1188Arg
ENST00000269571.9:c.3562G>C	ENSP00000269571.4:p.Gly1188Arg
ENST00000406381.6:c.3472G>C	ENSP00000385185.2:p.Gly1158Arg
ENST00000445658.6:c.2734G>C	ENSP00000404047.2:p.Gly912Arg
ENST00000541774.5:c.3517G>C	ENSP00000446466.1:p.Gly1173Arg
ENST00000578373.5:c.*3352G>C	ENSP00000463427.1:n.*3352G>C
ENST00000584450.5:c.*141G>C	ENSP00000463714.1:n.*141G>C
ENST00000584601.5:c.3472G>C	ENSP00000462438.1:p.Gly1158Arg
NM_001005862.2:c.3472G>C , LRG_724t1:c.3472G>C	NP_001005862.1:p.Gly1158Arg
NM_001289936.1:c.3517G>C , LRG_724t4:c.3517G>C	NP_001276865.1:p.Gly1173Arg
NM_001289937.1:c.*141G>C	NP_001276866.1:n.*141G>C
NM_004448.3:c.3562G>C , LRG_724t2:c.3562G>C	NP_004439.2:p.Gly1188Arg
NR_110535.1:n.3886G>C
XM_024450641.1:c.3700G>C	XP_024306409.1:p.Gly1234Arg
XM_024450642.1:c.3655G>C	XP_024306410.1:p.Gly1219Arg
XM_024450643.1:c.3610G>C	XP_024306411.1:p.Gly1204Arg
NM_001005862.3:c.3472G>C	NP_001005862.1:p.Gly1158Arg
NM_001289936.2:c.3517G>C	NP_001276865.1:p.Gly1173Arg
NM_001289937.2:c.*141G>C	NP_001276866.1:n.*141G>C
NM_001382782.1:c.3472G>C	NP_001369711.1:p.Gly1158Arg
NM_001382783.1:c.3472G>C	NP_001369712.1:p.Gly1158Arg
NM_001382784.1:c.3679G>C	NP_001369713.1:p.Gly1227Arg
NM_001382785.1:c.3664G>C	NP_001369714.1:p.Gly1222Arg
NM_001382786.1:c.3643G>C	NP_001369715.1:p.Gly1215Arg
NM_001382787.1:c.3637G>C	NP_001369716.1:p.Gly1213Arg
NM_001382788.1:c.3592G>C	NP_001369717.1:p.Gly1198Arg
NM_001382789.1:c.3583G>C	NP_001369718.1:p.Gly1195Arg
NM_001382790.1:c.3559G>C	NP_001369719.1:p.Gly1187Arg
NM_001382791.1:c.3553G>C	NP_001369720.1:p.Gly1185Arg
NM_001382792.1:c.3526G>C	NP_001369721.1:p.Gly1176Arg
NM_001382793.1:c.3520G>C	NP_001369722.1:p.Gly1174Arg
NM_001382794.1:c.3520G>C	NP_001369723.1:p.Gly1174Arg
NM_001382795.1:c.3514G>C	NP_001369724.1:p.Gly1172Arg
NM_001382796.1:c.3475G>C	NP_001369725.1:p.Gly1159Arg
NM_001382797.1:c.3463G>C	NP_001369726.1:p.Gly1155Arg
NM_001382798.1:c.3406G>C	NP_001369727.1:p.Gly1136Arg
NM_001382799.1:c.3382G>C	NP_001369728.1:p.Gly1128Arg
NM_001382800.1:c.3376G>C	NP_001369729.1:p.Gly1126Arg
NM_001382801.1:c.3358G>C	NP_001369730.1:p.Gly1120Arg
NM_001382802.1:c.3304G>C	NP_001369731.1:p.Gly1102Arg
NM_001382803.1:c.*141G>C	NP_001369732.1:n.*141G>C
NM_001382804.1:c.2734G>C	NP_001369733.1:p.Gly912Arg
NM_001382805.1:c.2611G>C	NP_001369734.1:p.Gly871Arg
NM_001382806.1:c.2524G>C	NP_001369735.1:p.Gly842Arg
NM_004448.4:c.3562G>C MANE Select	NP_004439.2:p.Gly1188Arg
NR_110535.2:n.3800G>C