Canonical Allele Identifier: CA399313801

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143305238
• MyVariant Identifiers: chr17:g.37884116A>G (hg19) ; chr17:g.39727863A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727863A>G , CM000679.2:g.39727863A>G	GRCh38
NC_000017.10:g.37884116A>G , CM000679.1:g.37884116A>G	GRCh37
NC_000017.9:g.35137642A>G	NCBI36
NG_007503.1:g.44724A>G , LRG_724:g.44724A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3587A>G MANE Select	ENSP00000269571.4:p.Tyr1196Cys
ENST00000269571.9:c.3587A>G	ENSP00000269571.4:p.Tyr1196Cys
ENST00000406381.6:c.3497A>G	ENSP00000385185.2:p.Tyr1166Cys
ENST00000445658.6:c.2759A>G	ENSP00000404047.2:p.Tyr920Cys
ENST00000541774.5:c.3542A>G	ENSP00000446466.1:p.Tyr1181Cys
ENST00000578373.5:c.*3377A>G	ENSP00000463427.1:n.*3377A>G
ENST00000584450.5:c.*166A>G	ENSP00000463714.1:n.*166A>G
ENST00000584601.5:c.3497A>G	ENSP00000462438.1:p.Tyr1166Cys
NM_001005862.2:c.3497A>G , LRG_724t1:c.3497A>G	NP_001005862.1:p.Tyr1166Cys
NM_001289936.1:c.3542A>G , LRG_724t4:c.3542A>G	NP_001276865.1:p.Tyr1181Cys
NM_001289937.1:c.*166A>G	NP_001276866.1:n.*166A>G
NM_004448.3:c.3587A>G , LRG_724t2:c.3587A>G	NP_004439.2:p.Tyr1196Cys
NR_110535.1:n.3911A>G
XM_024450641.1:c.3725A>G	XP_024306409.1:p.Tyr1242Cys
XM_024450642.1:c.3680A>G	XP_024306410.1:p.Tyr1227Cys
XM_024450643.1:c.3635A>G	XP_024306411.1:p.Tyr1212Cys
NM_001005862.3:c.3497A>G	NP_001005862.1:p.Tyr1166Cys
NM_001289936.2:c.3542A>G	NP_001276865.1:p.Tyr1181Cys
NM_001289937.2:c.*166A>G	NP_001276866.1:n.*166A>G
NM_001382782.1:c.3497A>G	NP_001369711.1:p.Tyr1166Cys
NM_001382783.1:c.3497A>G	NP_001369712.1:p.Tyr1166Cys
NM_001382784.1:c.3704A>G	NP_001369713.1:p.Tyr1235Cys
NM_001382785.1:c.3689A>G	NP_001369714.1:p.Tyr1230Cys
NM_001382786.1:c.3668A>G	NP_001369715.1:p.Tyr1223Cys
NM_001382787.1:c.3662A>G	NP_001369716.1:p.Tyr1221Cys
NM_001382788.1:c.3617A>G	NP_001369717.1:p.Tyr1206Cys
NM_001382789.1:c.3608A>G	NP_001369718.1:p.Tyr1203Cys
NM_001382790.1:c.3584A>G	NP_001369719.1:p.Tyr1195Cys
NM_001382791.1:c.3578A>G	NP_001369720.1:p.Tyr1193Cys
NM_001382792.1:c.3551A>G	NP_001369721.1:p.Tyr1184Cys
NM_001382793.1:c.3545A>G	NP_001369722.1:p.Tyr1182Cys
NM_001382794.1:c.3545A>G	NP_001369723.1:p.Tyr1182Cys
NM_001382795.1:c.3539A>G	NP_001369724.1:p.Tyr1180Cys
NM_001382796.1:c.3500A>G	NP_001369725.1:p.Tyr1167Cys
NM_001382797.1:c.3488A>G	NP_001369726.1:p.Tyr1163Cys
NM_001382798.1:c.3431A>G	NP_001369727.1:p.Tyr1144Cys
NM_001382799.1:c.3407A>G	NP_001369728.1:p.Tyr1136Cys
NM_001382800.1:c.3401A>G	NP_001369729.1:p.Tyr1134Cys
NM_001382801.1:c.3383A>G	NP_001369730.1:p.Tyr1128Cys
NM_001382802.1:c.3329A>G	NP_001369731.1:p.Tyr1110Cys
NM_001382803.1:c.*166A>G	NP_001369732.1:n.*166A>G
NM_001382804.1:c.2759A>G	NP_001369733.1:p.Tyr920Cys
NM_001382805.1:c.2636A>G	NP_001369734.1:p.Tyr879Cys
NM_001382806.1:c.2549A>G	NP_001369735.1:p.Tyr850Cys
NM_004448.4:c.3587A>G MANE Select	NP_004439.2:p.Tyr1196Cys
NR_110535.2:n.3825A>G