Canonical Allele Identifier: CA399312727

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143256793
• MyVariant Identifiers: chr17:g.37883764G>T (hg19) ; chr17:g.39727511G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727511G>T , CM000679.2:g.39727511G>T	GRCh38
NC_000017.10:g.37883764G>T , CM000679.1:g.37883764G>T	GRCh37
NC_000017.9:g.35137290G>T	NCBI36
NG_007503.1:g.44372G>T , LRG_724:g.44372G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3376G>T MANE Select	ENSP00000269571.4:p.Gly1126Cys
ENST00000269571.9:c.3376G>T	ENSP00000269571.4:p.Gly1126Cys
ENST00000406381.6:c.3286G>T	ENSP00000385185.2:p.Gly1096Cys
ENST00000445658.6:c.2548G>T	ENSP00000404047.2:p.Gly850Cys
ENST00000541774.5:c.3331G>T	ENSP00000446466.1:p.Gly1111Cys
ENST00000578373.5:c.*3166G>T	ENSP00000463427.1:n.*3166G>T
ENST00000584450.5:c.3160-178G>T	ENSP00000463714.1:n.3160-178G>T
ENST00000584601.5:c.3286G>T	ENSP00000462438.1:p.Gly1096Cys
NM_001005862.2:c.3286G>T , LRG_724t1:c.3286G>T	NP_001005862.1:p.Gly1096Cys
NM_001289936.1:c.3331G>T , LRG_724t4:c.3331G>T	NP_001276865.1:p.Gly1111Cys
NM_001289937.1:c.3160-178G>T	NP_001276866.1:n.3160-178G>T
NM_004448.3:c.3376G>T , LRG_724t2:c.3376G>T	NP_004439.2:p.Gly1126Cys
NR_110535.1:n.3700G>T
XM_024450641.1:c.3514G>T	XP_024306409.1:p.Gly1172Cys
XM_024450642.1:c.3469G>T	XP_024306410.1:p.Gly1157Cys
XM_024450643.1:c.3424G>T	XP_024306411.1:p.Gly1142Cys
NM_001005862.3:c.3286G>T	NP_001005862.1:p.Gly1096Cys
NM_001289936.2:c.3331G>T	NP_001276865.1:p.Gly1111Cys
NM_001289937.2:c.3160-178G>T	NP_001276866.1:n.3160-178G>T
NM_001382782.1:c.3286G>T	NP_001369711.1:p.Gly1096Cys
NM_001382783.1:c.3286G>T	NP_001369712.1:p.Gly1096Cys
NM_001382784.1:c.3493G>T	NP_001369713.1:p.Gly1165Cys
NM_001382785.1:c.3478G>T	NP_001369714.1:p.Gly1160Cys
NM_001382786.1:c.3457G>T	NP_001369715.1:p.Gly1153Cys
NM_001382787.1:c.3451G>T	NP_001369716.1:p.Gly1151Cys
NM_001382788.1:c.3406G>T	NP_001369717.1:p.Gly1136Cys
NM_001382789.1:c.3397G>T	NP_001369718.1:p.Gly1133Cys
NM_001382790.1:c.3373G>T	NP_001369719.1:p.Gly1125Cys
NM_001382791.1:c.3367G>T	NP_001369720.1:p.Gly1123Cys
NM_001382792.1:c.3340G>T	NP_001369721.1:p.Gly1114Cys
NM_001382793.1:c.3334G>T	NP_001369722.1:p.Gly1112Cys
NM_001382794.1:c.3334G>T	NP_001369723.1:p.Gly1112Cys
NM_001382795.1:c.3328G>T	NP_001369724.1:p.Gly1110Cys
NM_001382796.1:c.3289G>T	NP_001369725.1:p.Gly1097Cys
NM_001382797.1:c.3277G>T	NP_001369726.1:p.Gly1093Cys
NM_001382798.1:c.3220G>T	NP_001369727.1:p.Gly1074Cys
NM_001382799.1:c.3196G>T	NP_001369728.1:p.Gly1066Cys
NM_001382800.1:c.3190G>T	NP_001369729.1:p.Gly1064Cys
NM_001382801.1:c.3172G>T	NP_001369730.1:p.Gly1058Cys
NM_001382802.1:c.3118G>T	NP_001369731.1:p.Gly1040Cys
NM_001382803.1:c.3118-178G>T	NP_001369732.1:n.3118-178G>T
NM_001382804.1:c.2548G>T	NP_001369733.1:p.Gly850Cys
NM_001382805.1:c.2425G>T	NP_001369734.1:p.Gly809Cys
NM_001382806.1:c.2338G>T	NP_001369735.1:p.Gly780Cys
NM_004448.4:c.3376G>T MANE Select	NP_004439.2:p.Gly1126Cys
NR_110535.2:n.3614G>T