Canonical Allele Identifier: CA399313791

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3587A>C MANE Select	ENSP00000269571.4:p.Tyr1196Ser
ENST00000269571.9:c.3587A>C	ENSP00000269571.4:p.Tyr1196Ser
ENST00000406381.6:c.3497A>C	ENSP00000385185.2:p.Tyr1166Ser
ENST00000445658.6:c.2759A>C	ENSP00000404047.2:p.Tyr920Ser
ENST00000541774.5:c.3542A>C	ENSP00000446466.1:p.Tyr1181Ser
ENST00000578373.5:c.*3377A>C	ENSP00000463427.1:n.*3377A>C
ENST00000584450.5:c.*166A>C	ENSP00000463714.1:n.*166A>C
ENST00000584601.5:c.3497A>C	ENSP00000462438.1:p.Tyr1166Ser
NM_001005862.2:c.3497A>C , LRG_724t1:c.3497A>C	NP_001005862.1:p.Tyr1166Ser
NM_001289936.1:c.3542A>C , LRG_724t4:c.3542A>C	NP_001276865.1:p.Tyr1181Ser
NM_001289937.1:c.*166A>C	NP_001276866.1:n.*166A>C
NM_004448.3:c.3587A>C , LRG_724t2:c.3587A>C	NP_004439.2:p.Tyr1196Ser
NR_110535.1:n.3911A>C
XM_024450641.1:c.3725A>C	XP_024306409.1:p.Tyr1242Ser
XM_024450642.1:c.3680A>C	XP_024306410.1:p.Tyr1227Ser
XM_024450643.1:c.3635A>C	XP_024306411.1:p.Tyr1212Ser
NM_001005862.3:c.3497A>C	NP_001005862.1:p.Tyr1166Ser
NM_001289936.2:c.3542A>C	NP_001276865.1:p.Tyr1181Ser
NM_001289937.2:c.*166A>C	NP_001276866.1:n.*166A>C
NM_001382782.1:c.3497A>C	NP_001369711.1:p.Tyr1166Ser
NM_001382783.1:c.3497A>C	NP_001369712.1:p.Tyr1166Ser
NM_001382784.1:c.3704A>C	NP_001369713.1:p.Tyr1235Ser
NM_001382785.1:c.3689A>C	NP_001369714.1:p.Tyr1230Ser
NM_001382786.1:c.3668A>C	NP_001369715.1:p.Tyr1223Ser
NM_001382787.1:c.3662A>C	NP_001369716.1:p.Tyr1221Ser
NM_001382788.1:c.3617A>C	NP_001369717.1:p.Tyr1206Ser
NM_001382789.1:c.3608A>C	NP_001369718.1:p.Tyr1203Ser
NM_001382790.1:c.3584A>C	NP_001369719.1:p.Tyr1195Ser
NM_001382791.1:c.3578A>C	NP_001369720.1:p.Tyr1193Ser
NM_001382792.1:c.3551A>C	NP_001369721.1:p.Tyr1184Ser
NM_001382793.1:c.3545A>C	NP_001369722.1:p.Tyr1182Ser
NM_001382794.1:c.3545A>C	NP_001369723.1:p.Tyr1182Ser
NM_001382795.1:c.3539A>C	NP_001369724.1:p.Tyr1180Ser
NM_001382796.1:c.3500A>C	NP_001369725.1:p.Tyr1167Ser
NM_001382797.1:c.3488A>C	NP_001369726.1:p.Tyr1163Ser
NM_001382798.1:c.3431A>C	NP_001369727.1:p.Tyr1144Ser
NM_001382799.1:c.3407A>C	NP_001369728.1:p.Tyr1136Ser
NM_001382800.1:c.3401A>C	NP_001369729.1:p.Tyr1134Ser
NM_001382801.1:c.3383A>C	NP_001369730.1:p.Tyr1128Ser
NM_001382802.1:c.3329A>C	NP_001369731.1:p.Tyr1110Ser
NM_001382803.1:c.*166A>C	NP_001369732.1:n.*166A>C
NM_001382804.1:c.2759A>C	NP_001369733.1:p.Tyr920Ser
NM_001382805.1:c.2636A>C	NP_001369734.1:p.Tyr879Ser
NM_001382806.1:c.2549A>C	NP_001369735.1:p.Tyr850Ser
NM_004448.4:c.3587A>C MANE Select	NP_004439.2:p.Tyr1196Ser
NR_110535.2:n.3825A>C